Donor Profile : Donor 5426

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Retired Donor

This donor is no longer active in the program. The number of vials available represents the remainder of the donor's inventory.

Donor ID: 5426

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Meet The Donor

It's quite an accomplishment to obtain Eagle Scout status, and Donor 5426 knows it. He also draws and plays piano and guitar, in addition to attending a prestigious engineering school. He loves storytelling and the emotions and memories a good story will invoke.

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Donor 5426 has more photos.

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Genetic Testing Performed: Please review the list of genetic tests performed before choosing a donor because donors have different levels of testing. Genetics is very complicated and testing can only reduce but not eliminate the risk of a donor being a carrier of a particular condition.


Any potential new health information will be indicated here. Please check periodically for medical updates. This profile is current as of:
October 19, 2025 1:35 AM EST


Document ID: 5AC6522058988C677BEE2661897B4F7BC6226FDEC78359E9DD8EA4D70FFEE734

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Donor's "Name": Clay

Year of Birth: 1992

Marital Status: Single

Number of Children: 0

Occupation:
(last reported)
Student

Education: none

Blood Type: O +

Nationality:
(self reported)
Maternal: English
Scottish
Indigenous American
Paternal: English
Scottish
Indigenous American

Race: White Or Caucasian

CMV Status: POS
Learn More

Last Medical History Update: 05/07/2020

  • Reported Pregnancy/Birth
  • xyIdentity Disclosure
  • Available Inventory
  • Retired

ADDITIONAL DONOR DETAILS

  • Height:
    5'7" (170.18 cm)
    Weight:
    140 lbs (63 kg)
    Eye Color:
    Blue/Grey
    Hair Color:
    Blonde, Dark
    Hair Texture:
    Fine
    Hair Loss:
    None
    Hair Type:
    Average
    Body Build:
    Small
    Freckles:
    Few
    Skin Tone:
    Fair
  • Over the years, Xytex has expanded genetic testing of donors as genetic knowledge and technology have advanced. As a result, not all donors have been tested for the same conditions or with the same methods. For more information about genetic testing view our Genetics FAQs.

    This donor has been evaluated for carrier status of the listed conditions. A negative result reduces, but does not eliminate, the likelihood of the donor being a carrier. If you are a known carrier of a genetic condition, please use the advanced search features to find donors who have tested negative for the condition(s) that you carry. Click the relevant link below to download the donor's test reports to share with your physician and/or genetic counselor.

    This donor's carrier testing included 107 genes.

    21-Alpha-Hydroxylase-Deficient Congenital Adrenal Hyperplasia (CYP21A2)
    No disease-causing variants detected
    3-Methylglutaconic Aciduria Type III also known as Costeff Optic Atrophy (OPA3)
    No disease-causing variants detected
    Achromatopsia (CNGB3)
    No disease-causing variants detected
    Alkaptonuria (HGD)
    No disease-causing variants detected
    Alpha-1 Antitrypsin Deficiency (SERPINA1)
    No disease-causing variants detected
    Alpha-Mannosidosis (MAN2B1)
    No disease-causing variants detected
    Alpha-Thalassemia (HBA1/HBA2)
    No disease-causing mutations detected; normal red blood cell indices and hemoglobin analysis
    Andermann Syndrome (SLC12A6)
    No disease-causing variants detected
    Aspartylglucosaminuria (AGA)
    No disease-causing variants detected
    Ataxia With Vitamin E Deficiency (TTPA)
    No disease-causing variants detected
    Ataxia-Telangiectasia (ATM)
    No disease-causing variants detected
    Bardet-Biedl Syndrome, BBS1-Related (BBS1)
    No disease-causing variants detected
    Bardet-Biedl Syndrome, BBS10-Related (BBS10)
    No disease-causing variants detected
    Beta-Thalassemia, Sickle Cell Disease, and Beta-Globin Disorders (HBB)
    No disease-causing mutations detected; normal red blood cell indices and hemoglobin analysis
    Biotinidase Deficiency (BTD)
    No disease-causing variants detected
    Bloom Syndrome (BLM)
    No disease-causing variants detected
    Canavan Disease (ASPA)
    No disease-causing variants detected
    Carnitine Palmitoyltransferase IA Deficiency (CPT1A)
    No disease-causing variants detected
    Carnitine Palmitoyltransferase II Deficiency (CPT2)
    No disease-causing variants detected
    Cartilage-Hair Hypoplasia (RMRP)
    No disease-causing variants detected
    Choroidemia, X-Linked (CHM)
    No disease-causing variants detected
    Chromosome Analysis (Karyotype)
    Normal male karyotype
    Citrullinemia Type 1 (ASS1)
    No disease-causing variants detected
    Cohen Syndrome (VPS13B)
    No disease-causing variants detected
    Combined Pituitary Hormone Deficiency 2 (PROP1)
    No disease-causing variants detected
    Congenital Disorder of Glycosylation Type 1a, PMM2-Related (PMM2)
    No disease-causing variants detected
    Congenital Disorder of Glycosylation Type 1b (MPI)
    No disease-causing variants detected
    Cystic Fibrosis and Other CFTR-Related Disorders (CFTR)
    No disease-causing variants detected
    Cystinosis (CTNS)
    No disease-causing variants detected
    D-Bifunctional Protein Deficiency (HSD17B4)
    No disease-causing variants detected
    Developmental and Epileptic Encephalopathy 4 (STXBP1)
    No disease-causing variants detected
    Dihydropyrimidine Dehydrogenase Deficiency also known as Hereditary Thymine-Uraciluria (DPYD)
    No disease-causing variants detected
    Factor XI Deficiency (F11)
    No disease-causing variants detected
    Familial Dysautonomia (IKBKAP)
    No disease-causing variants detected
    Familial Hyperinsulinism and Other ABCC8-Related Disorders (ABCC8)
    No disease-causing variants detected
    Familial Mediterranean Fever (MEFV)
    No disease-causing variants detected
    Fanconi Anemia Type C (FANCC)
    No disease-causing variants detected
    Galactosemia, GALT-Related (GALT)
    No disease-causing variants detected
    Gaucher Disease (GBA)
    No disease-causing variants detected
    GJB2-Related DFNB1 Nonsyndromic Hearing Loss and Deafness (GJB2)
    No disease-causing variants detected
    Glutaric Acidemia Type 1 (GCDH)
    No disease-causing variants detected
    Glycogen Storage Disease Type Ia (G6PC)
    No disease-causing variants detected
    Glycogen Storage Disease Type Ib (SLC37A4)
    No disease-causing variants detected
    Glycogen Storage Disease Type III (AGL)
    No disease-causing variants detected
    Glycogen Storage Disease Type V (PYGM)
    No disease-causing variants detected
    GRACILE Syndrome (BCS1L)
    No disease-causing variants detected
    Hereditary Fructose Intolerance (ALDOB)
    No disease-causing variants detected
    Homocystinuria (CBS)
    No disease-causing variants detected
    Hypophosphatasia, Autosomal Recessive (ALPL)
    No disease-causing variants detected
    Inclusion Body Myopathy 2 (GNE)
    No disease-causing variants detected
    Isovaleric Acidemia (IVD)
    No disease-causing variants detected
    Joubert Syndrome 2 (TMEM216)
    No disease-causing variants detected
    Junctional Epidermolysis Bullosa (LAMA3)
    No disease-causing variants detected
    Junctional Epidermolysis Bullosa (LAMB3)
    No disease-causing variants detected
    Junctional Epidermolysis Bullosa (LAMC2)
    No disease-causing variants detected
    Juvenile Retinoschisis, X-Linked (RS1)
    No disease-causing variants detected
    Krabbe Disease (GALC)
    No disease-causing variants detected
    Limb-Girdle Muscular Dystrophy Type 2D also known as Alpha-Sarcoglycanopathy (SGCA)
    No disease-causing variants detected
    Limb-Girdle Muscular Dystrophy Type 2E also known as Beta-Sarcoglycanopathy (SGCB)
    No disease-causing variants detected
    Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency (HADHA)
    No disease-causing variants detected
    Maple Syrup Urine Disease Type 1B (BCKDHB)
    No disease-causing variants detected
    Maple Syrup Urine Disease Type 3 also known as Dihyrolipoamide Dehydrogenase Deficiency (DLD)
    No disease-causing variants detected
    Medium Chain Acyl-CoA Dehydrogenase Deficiency (ACADM)
    No disease-causing variants detected
    Megalencephalic Leukoencephalopathy With Subcortical Cysts Type 1 (MLC1)
    No disease-causing variants detected
    Metachromatic Leukodystrophy (ARSA)
    No disease-causing variants detected
    Mucolipidosis Type IV (MCOLN1)
    No disease-causing variants detected
    Mucopolysaccharidosis Type I also known as Hurler Syndrome (IDUA)
    No disease-causing variants detected
    Muscle-Eye-Brain Disease (POMGNT1)
    No disease-causing variants detected
    Nemaline Myopathy 2 (NEB)
    No disease-causing variants detected
    Nephrotic Syndrome, NPHS1-Related also known as Congenital Finnish Nephrosis (NPHS1)
    No disease-causing variants detected
    Nephrotic Syndrome, NPHS2-Related also known as Steroid-Resistant Nephrotic Syndrome (NPHS2)
    No disease-causing variants detected
    Neuronal Ceroid-Lipofuscinosis, CLN3-Related (CLN3)
    No disease-causing variants detected
    Neuronal Ceroid-Lipofuscinosis, CLN5-Related (CLN5)
    No disease-causing variants detected
    Neuronal Ceroid-Lipofuscinosis, CLN8-Related also known as Northern Epilepsy (CLN8)
    No disease-causing variants detected
    Neuronal Ceroid-Lipofuscinosis, PPT1-Related (PPT1)
    No disease-causing variants detected
    Neuronal Ceroid-Lipofuscinosis, TPP1-Related (TPP1)
    No disease-causing variants detected
    Niemann-Pick Disease Type A/B (SMPD1)
    No disease-causing variants detected
    Niemann-Pick Disease Type A/B (SMPD1)
    No disease-causing variants detected
    Niemann-Pick Disease Type C, NPC1-Related (NPC1)
    No disease-causing variants detected
    Nijmegen Breakage Syndrome (NBN)
    No disease-causing variants detected
    Osteochondrodysplasias, Sulfate Transporter-Related (SLC26A2)
    No disease-causing variants detected
    Pendred Syndrome (SLC26A4)
    No disease-causing variants detected
    Phenylalanine Hydroxylase Deficiency also known as Phenylketonuria (PAH)
    No disease-causing variants detected
    Polycystic Kidney Disease, Autosomal Recessive (PKHD1)
    No disease-causing variants detected
    Polyglandular Autoimmune Syndrome Type 1 (AIRE)
    No disease-causing variants detected
    Pompe Disease also known as Glycogen Storage Disease Type II (GAA)
    No disease-causing variants detected
    Primary Carnitine Deficiency (SLC22A5)
    No disease-causing variants detected
    Primary Hyperoxaluria Type 1 (AGXT)
    No disease-causing variants detected
    Primary Hyperoxaluria Type 2 (GRHPR)
    No disease-causing variants detected
    Pseudocholinesterase Deficiency (BCHE)
    No disease-causing variants detected
    Pycnodysostosis (CTSK)
    No disease-causing variants detected
    Rhizomelic Chondrodysplasia Punctata Type 1 (PEX7)
    No disease-causing variants detected
    Salla Disease (SLC17A5)
    No disease-causing variants detected
    SCN9A-Related Disorders (SCN9A)
    No disease-causing variants detected
    Segawa Syndrome (TH)
    No disease-causing variants detected
    Short Chain Acyl-CoA Dehydrogenase Deficiency (ACADS)
    No disease-causing variants detected
    Sjogren-Larsson Syndrome (ALDH3A2)
    No disease-causing variants detected
    Smith-Lemli-Opitz Syndrome (DHCR7)
    No disease-causing variants detected
    Spastic Ataxia of Charlevoix-Saguenay, Autosomal Recessive (SACS)
    No disease-causing variants detected
    Spinal Muscular Atrophy (SMN1)
    No disease-causing mutations detected (2 copies detected)
    Steroid-Resistant Nephrotic Syndrome
    See results for Nephrotic Syndrome, NPHS2-Related (NPHS2)
    Tay-Sachs Disease also known as Hexosaminidase A Deficiency (HEXA)
    No disease-causing variants detected
    Tyrosinemia Type 1 (FAH)
    No disease-causing variants detected
    Usher Syndrome Type IF (PCDH15)
    No disease-causing variants detected
    Usher Syndrome Type IIIA (CLRN1)
    No disease-causing variants detected
    Very Long Chain Acyl-CoA Dehydrogenase Deficiency (ACADVL)
    No disease-causing variants detected
    Wilson Disease (ATP7B)
    No disease-causing variants detected
    Zellweger Spectrum Disorder, PEX1-Related (PEX1)
    No disease-causing variants detected
  • Medication Allergy:
    No
    Food Allergy:
    No
    Pet Allergy:
    No
    Hay Fever Allergy:
    No
    Insect Allergy:
    No
    Vaccine Allergy:
    No
    Healthy Teeth:
    Yes
    Braces:
    Yes
    Back Problems:
    No
    Bronchitis:
    No
    Chicken Pox:
    No
    Chicken Pox Age:
    Vertigo:
    No
    Eyesight Correction:
    Yes
    Near or Far Sighted:
    Nearsighted
    Skin Infection:
    No
    Gallstones:
    No
    Removed Gall Bladder:
    No
    Hernia:
    No
    Mumps:
    No
    Measles:
    No
    Measles Age:
    German Measles:
    No
    German Measles Age:
    Sinus Infection:
    Yes
    Stomach Ulcers:
    No
  • Skills, Hobbies and Interests:
    I can whistle, weld metal together, roll sushi, and hold my breath for over a minute. I run long distance for exercise and am also a GT scholarship athlete for cheerleader.

  • In School:
    Yes
    In School Major:
    Computer science
    Post Graduate:
    No
    Training Type:
    College Degrees:
    none
  • The following medical conditions apply to the donor and his BLOOD RELATIVES ONLY (grandparents, parents, aunts, uncles, cousins, brothers, sisters, nieces, nephews and children of the donor).

    If a donor answers "yes" to any high-risk question on his Medical History Questionnaire, the donor is ineligible.

    Autoimmune Diseases Yes No Which
    Relative
    Father's
    Side
    Mother's
    Side
    Age of
    Onset
    CREST Syndrome X
    Lupus X
    Scleroderma X
    Sjogren's Syndrome X
    Blood Diseases Yes No Which
    Relative
    Father's
    Side
    Mother's
    Side
    Age of
    Onset
    Anemia X
    Fanconi Anemia X
    Hemophilia X
    Immunodeficiency X
    Leukemia X
    Sickle Cell X
    Thalassemia X
    Von Willebrand's disease X
    Cancer Yes No Which
    Relative
    Father's
    Side
    Mother's
    Side
    Age of
    Onset
    Cancer (Breast) X
    Cancer (Colon) X
    Cancer (Leukemia) X
    Cancer (Lung) X
    Cancer (Other) X
    Cancer (Skin) X Grandfather X 94
    Lymphoma X
    Melanoma X
    Prostate X
    Tumor X
    Cardio Vascular Diseases Yes No Which
    Relative
    Father's
    Side
    Mother's
    Side
    Age of
    Onset
    Congenital Heart Disease X
    Heart Attack X
    Heart Disease X
    High Blood Pressure X
    High Cholesterol/Triglycerides X
    Stroke X
    Cardio Vascular (Other) X
    Congenital Malformations Yes No Which
    Relative
    Father's
    Side
    Mother's
    Side
    Age of
    Onset
    Deviated Septum X
    Malformations (Cleft Lip) X
    Malformations (Cleft Palate) X
    Malformations (Club Foot) X
    Malformations (Hypospadias) X
    Malformations (Other) X
    Malformations (Polydactyly) X
    Malformations (Syndactyly) X
    Undescended Testicles X
    Gastro-Intestinal Diseases Yes No Which
    Relative
    Father's
    Side
    Mother's
    Side
    Age of
    Onset
    Gallstones X
    GI (Crohn's) X
    GI (Diverticulitis) X
    GI (Other) X
    GI (Pyloric Stenosis) X
    GI (Ulcerative Colitis) X
    GI (Ulcers) X
    Hemochromatosis X
    Hepatitis X
    Kidney Diseases Yes No Which
    Relative
    Father's
    Side
    Mother's
    Side
    Age of
    Onset
    Adrenal Hyperplasia X
    Born with 1 kidney X
    Kidney (Other) X
    Kidney disease or urinary tract disorder X
    Kidney Disorder X
    Polycystic Kidney Disease X
    Progressive Kidney Disease X
    Mental Health Yes No Which
    Relative
    Father's
    Side
    Mother's
    Side
    Age of
    Onset
    Anxiety disorder X
    Mental (Depression) X
    Mental (Manic Depressive) X
    Mental (Schizophrenia) X
    Mental Retardation X
    Obsessive-compulsive disorder X
    Metabolic/Endrocrine Dis. Yes No Which
    Relative
    Father's
    Side
    Mother's
    Side
    Age of
    Onset
    Diabetes (Insulin Dependent) X
    Diabetes (Non-Insulin Dependent) X
    Galactosemia X
    Gaucher's disease X
    Goiter X
    Hypoglycemia X
    Maple Syrup disease X
    PKU or Inherited Metabolic Disorder X
    Tay Sachs X
    Thyroid Disorder X
    Muscular/Bones/Joint Disease Yes No Which
    Relative
    Father's
    Side
    Mother's
    Side
    Age of
    Onset
    Achondroplasia (Dwarfism) X
    Arthritis (Other) X
    Congenital Hip Disease X
    Gout X
    Loss of Muscle Coordination X
    Marfan's Disease X
    Muscular Dystrophy X
    Osteoarthritis X
    Osteoporosis X
    Rheumatoid Arthritis X Grandmother X 77
    Scoliosis X
    Spinal Muscular Atrophy X
    Neurological Diseases Yes No Which
    Relative
    Father's
    Side
    Mother's
    Side
    Age of
    Onset
    Learning Disorder: ADD, ADHD, Dyslexia X
    Autism/ Asperger X
    Canavan's disease X
    Cerebral Palsy X
    Dementia X
    Disorders of the spinal cord X
    Dyslexia X
    Familial dysautonomia X
    Lesch-Nyhan Syndrome X
    Migraines X Mother X 56
    Mucolipidosis type IV X
    Neurologic (Alzheimer) X
    Neurologic (Creutzfeldt-Jakob Disease) X
    Neurologic (Epilepsy) X
    Neurologic (Guillain Barre) X
    Neurologic (Huntington's) X
    Neurologic (JC Virus) X
    Neurologic (Lou Gehrig's Disease) X
    Neurologic (Multiple Sclerosis) X
    Neurologic (Neural Tube Defect) X
    Neurologic (Neurofibromatosis) X
    Neurologic (Parkinson's Disease) X
    Neurologic (Subacute Sclerosing Panencephalitis) X
    Nieman-Pick X
    Spongiform encephalopathy/prion disease X
    Tourette Syndrome X
    Other Yes No Which
    Relative
    Father's
    Side
    Mother's
    Side
    Age of
    Onset
    Alcoholism X Grandfather X 28
    Bloom syndrome X
    Cystic Fibrosis X
    Down Syndrome X
    Drug Abuse X
    Encephalitis: viral or of unknown origin X
    Fragile X X
    Klinefelter X
    Meningitis X
    Noonan or Turner Syndrome X
    Other - Early Death X
    Other - Inherited Genetic Condition X
    Other Disease/Condition X
    Premature Organ Degeneration X
    Radiation Exposure X
    SIDS X
    Toxic Chemical Exposure X
    Turner's Syndrome X
    West Nile (suspected or confirmed by lab testing) X
    Respiratory Disease Yes No Which
    Relative
    Father's
    Side
    Mother's
    Side
    Age of
    Onset
    Allergies (Drug) X
    Allergies (Food) Gluten X Mother X 54
    Allergies (Hay Fever) X
    Allergies (Insect) X
    Allergies (Other) X
    Allergies (Pet) Cats X Mother X 34
    Asthma X
    Emphysema X
    SARS X
    Tuberculosis X
    Sight/Sound/Smell Yes No Which
    Relative
    Father's
    Side
    Mother's
    Side
    Age of
    Onset
    Cataracts X Grandfather X 89
    Deafness X
    Deafness (before age 50) X
    Ear deformity X
    Eyesight (Blindness) X
    Eyesight (Red-Green Color Blindness) X
    Eyesight (Glaucoma) X
    Eyesight (Other) X
    Eyesight (Retinoblastoma) X
    Macular degeneration X
    Skin Yes No Which
    Relative
    Father's
    Side
    Mother's
    Side
    Age of
    Onset
    Albinism X
    Eczema X
    Pigmentation disorders (including Vitiligo) X
    Psoriasis X
    Skin Disease X
  • Information displayed in this profile is provided by the donor. Blank fields are intentional and indicate that the information is not available.

    FAMILY MEMBER: Father
    Hair Color: Black Eyesight:
    Freckles: Numerous Hair Texture: Thick
    Health Status: Good Skin Tone: Fair Dominant Hand:
    Year of Birth: 1949 Cause of Death: Hair Loss: Extensive Balding
    Height: 5'09" (175.26 cm) Age at Death: Body Hair: Straight
    Weight: 170 lbs. (77 kg) Occupation: Electrical Engineer Eye Color: Brown, Dark
    Half Siblings: No Education: College (Some) Body Build: Medium
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    Comments: He used to be a rock star; he’s a lead guitar player and pilot. Enjoys cars, computers, cycling, football, model and regular: planes and trains, and guns.
    FAMILY MEMBER: Mother
    Hair Color: Blonde, Dark Eyesight:
    Freckles: Few Hair Texture: Thin
    Health Status: Good Skin Tone: Fair Dominant Hand:
    Year of Birth: 1955 Cause of Death: Hair Loss:
    Height: 5'02" (157.48 cm) Age at Death: Body Hair: Straight
    Weight: 130 lbs. (59 kg) Occupation: Accountant Eye Color: Brown, Dark
    Half Siblings: No Education: Body Build: Small
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    Comments: Has correct vision. She has two green thumbs! Enjoys cooking, filing taxes, accounting, marketing, gardening and sewing.
  • Information displayed in this profile is provided by the donor. Blank fields are intentional and indicate that the information is not available.

    FAMILY MEMBER: Grandfather
    Hair Color: Blonde, Strawberry Eyesight:
    Freckles: Numerous Hair Texture: Thin
    Health Status: Skin Tone: Fair Dominant Hand:
    Year of Birth: 1919 Cause of Death: Old age Hair Loss: Extensive Balding
    Height: 5'08" (172.72 cm) Age at Death: 96 Body Hair: Straight
    Weight: 160 lbs. (72 kg) Occupation: Bank CEO Eye Color: Blue
    Half Siblings: Education: College Body Build: Medium
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    Comments: Had corrected vision. Enjoyed farming, sailing/boating, cooking, and RC airplanes.
    FAMILY MEMBER: Grandmother
    Hair Color: Brown, Medium Eyesight:
    Freckles: None Hair Texture: Thick
    Health Status: Fair Skin Tone: Fair Dominant Hand:
    Year of Birth: 1924 Cause of Death: Hair Loss:
    Height: 5'03" (160.02 cm) Age at Death: Body Hair: Curly
    Weight: 120 lbs. (54 kg) Occupation: School Teacher Eye Color: Brown, Light
    Half Siblings: Education: High School Body Build: Small
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    Comments: Has corrected vision. Enjoys painting, drawing, writing (published).
    FAMILY MEMBER: Uncle
    Hair Color: Eyesight:
    Freckles: Hair Texture:
    Health Status: Good Skin Tone: Dominant Hand:
    Year of Birth: 1952 Cause of Death: Hair Loss:
    Height: Age at Death: Body Hair:
    Weight: Occupation: Eye Color:
    Half Siblings: Education: Body Build:
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    FAMILY MEMBER: Aunt
    Hair Color: Eyesight:
    Freckles: Hair Texture:
    Health Status: Good Skin Tone: Dominant Hand:
    Year of Birth: 1955 Cause of Death: Hair Loss:
    Height: Age at Death: Body Hair:
    Weight: Occupation: Eye Color:
    Half Siblings: Education: Body Build:
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
  • Information displayed in this profile is provided by the donor. Blank fields are intentional and indicate that the information is not available.

    FAMILY MEMBER: Grandfather
    Hair Color: Black Eyesight:
    Freckles: None Hair Texture: Thick
    Health Status: Fair Skin Tone: Medium Dominant Hand:
    Year of Birth: 1922 Cause of Death: Hair Loss:
    Height: 5'10" (177.8 cm) Age at Death: Body Hair: Straight
    Weight: 180 lbs. (81 kg) Occupation: Eye Color: Brown, Dark
    Half Siblings: Education: High School Body Build: Medium
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    FAMILY MEMBER: Grandmother
    Hair Color: Brown, Dark Eyesight:
    Freckles: None Hair Texture: Thin
    Health Status: Fair Skin Tone: Fair Dominant Hand:
    Year of Birth: 1928 Cause of Death: Hair Loss:
    Height: 5'" (152.4 cm) Age at Death: Body Hair: Curly
    Weight: 110 lbs. (49 kg) Occupation: School Teacher Eye Color: Brown, Light
    Half Siblings: Education: High School Body Build: Small
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    Comments: Has corrected vision. Enjoys gardening, knitting, crocheting, and sewing.
    FAMILY MEMBER: Aunt
    Hair Color: Eyesight:
    Freckles: Hair Texture:
    Health Status: Good Skin Tone: Dominant Hand:
    Year of Birth: 1961 Cause of Death: Hair Loss:
    Height: Age at Death: Body Hair:
    Weight: Occupation: Eye Color:
    Half Siblings: Education: Body Build:
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    FAMILY MEMBER: Aunt
    Hair Color: Eyesight:
    Freckles: Hair Texture:
    Health Status: Good Skin Tone: Dominant Hand:
    Year of Birth: 1957 Cause of Death: Hair Loss:
    Height: Age at Death: Body Hair:
    Weight: Occupation: Eye Color:
    Half Siblings: Education: Body Build:
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    FAMILY MEMBER: Uncle
    Hair Color: Eyesight:
    Freckles: Hair Texture:
    Health Status: Good Skin Tone: Dominant Hand:
    Year of Birth: 1958 Cause of Death: Hair Loss:
    Height: Age at Death: Body Hair:
    Weight: Occupation: Eye Color:
    Half Siblings: Education: Body Build:
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:

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