COVID-19 Update - SSB is Open and Operational. Please view our Meet Robin (10179) – Open ID Donor – New Donor!
Back to Donor Search
- Eyes: Brown/Green
- Hair: Light Brown
- Height: 6'02"
- Weight (lbs): 160
- Blood: A Rh+
- CMV: -
- Ethnicity: Caucasian, German, Swedish
- Jewish Ancestry: No
- Education/Occupation: B.A. Economics / Student
- Live Birth / Pregnancy Confirmed: No
Test Results
- Extended Testing: Counsyl Fundamental Panel Plus (at least 21 conditions)
- Carrier For:
- Cystinosis: Carrier
- Pendred Syndrome: Carrier
- Results for Karyotyping / Spinal Muscular Atrophy:
- Karyotyping: 46, XY
- Spinal Muscular Atrophy: Copy number 2
- Results with No Disease Causing Mutations: View full list
- Cystic Fibrosis
- ABCC8-related Hyperinsulinism
- Achromatopsia
- Alkaptonuria
- Alpha-1 Antitrypsin Deficiency
- Alpha-mannosidosis
- Alpha Thalassemia
- Andermann Syndrome
- ARSACS
- Aspartylglycosaminuria
- Ataxia With Vitamin E Deficiency
- Ataxia-telangiectasia
- Autosomal Recessive Polycystic Kidney Disease
- Bardet-Biedl Syndrome, BBS1-related
- Bardet-Biedl Syndrome, BBS10-related
- Biotinidase Deficiency
- Bloom Syndrome
- Canavan Disease
- Carnitine Palmitoyltransferase 1A Deficiency
- Carnitine Palmitoyltransferase II Deficiency
- Cartilage-hair Hypoplasia
- Citrullinemia Type 1
- CLN3-related Neuronal Ceroid Lipofuscinosis
- CLN5-related Neuronal Ceroid Lipofuscinosis
- Cohen Syndrome
- 21-hydroxylase Deficient Congenital Adrenal Hyperplasia
- Congenital Disorder Of Glycosylation Type 1a
- Congenital Disorder Of Glycosylation Type 1b
- Congenital Finnish Nephrosis
- Costeff Optic Atrophy Syndrome
- D-bifunctional Protein Deficiency
- Factor XI Deficiency
- Familial Dysautonomia
- Familial Mediterranean Fever
- Fanconi Anemia Type C
- Galactosemia
- Gaucher Disease
- GJB2-related DFNB1 Nonsyndromic Hearing Loss And Deafness
- Glutaric Acidemia Type 1
- Glycogen Storage Disease Type Ia
- Glycogen Storage Disease Type Ib
- Glycogen Storage Disease Type III
- Glycogen Storage Disease Type V
- GRACILE Syndrome
- Hb Beta Chain-related Hemoglobinopathy (including Beta Thalassemia And Sickle Cell Disease)
- Hereditary Fructose Intolerance
- Hereditary Thymine-uraciluria
- Herlitz Junctional Epidermolysis Bullosa, LAMA3-related
- Herlitz Junctional Epidermolysis Bullosa, LAMB3-related
- Herlitz Junctional Epidermolysis Bullosa, LAMC2-related
- Hexosaminidase A Deficiency (including Tay-Sachs Disease)
- Homocystinuria Caused By Cystathionine Beta-synthase Deficiency
- Hurler Syndrome
- Hypophosphatasia, Autosomal Recessive
- Inclusion Body Myopathy 2
- Isovaleric Acidemia
- Joubert Syndrome 2
- Krabbe Disease
- Limb-girdle Muscular Dystrophy Type 2D
- Limb-girdle Muscular Dystrophy Type 2E
- Lipoamide Dehydrogenase Deficiency
- Long Chain 3-hydroxyacyl-CoA Dehydrogenase Deficiency
- Maple Syrup Urine Disease Type 1B
- Medium Chain Acyl-CoA Dehydrogenase Deficiency
- Megalencephalic Leukoencephalopathy With Subcortical Cysts
- Metachromatic Leukodystrophy
- Mucolipidosis IV
- Muscle-eye-brain Disease
- NEB-related Nemaline Myopathy
- Niemann-Pick Disease Type C
- Niemann-Pick Disease, SMPD1-associated
- Nijmegen Breakage Syndrome
- Northern Epilepsy
- PEX1-related Zellweger Syndrome Spectrum
- Phenylalanine Hydroxylase Deficiency
- Polyglandular Autoimmune Syndrome Type 1
- Pompe Disease
- PPT1-related Neuronal Ceroid Lipofuscinosis
- Primary Carnitine Deficiency
- Primary Hyperoxaluria Type 1
- Primary Hyperoxaluria Type 2
- PROP1-related Combined Pituitary Hormone Deficiency
- Pseudocholinesterase Deficiency
- Pycnodysostosis
- Rhizomelic Chondrodysplasia Punctata Type 1
- Salla Disease
- Segawa Syndrome
- Short Chain Acyl-CoA Dehydrogenase Deficiency
- Sjogren-Larsson Syndrome
- Smith-Lemli-Opitz Syndrome
- Steroid-resistant Nephrotic Syndrome
- Sulfate Transporter-related Osteochondrodysplasia
- TPP1-related Neuronal Ceroid Lipofuscinosis
- Tyrosinemia Type 1
- Usher Syndrome Type 1F
- Usher Syndrome Type 3
- Very Long Chain Acyl-CoA Dehydrogenase Deficiency
- Walker-Warburg Syndrome
- Wilson Disease
Donor Description
Robin is tall, standing at 6’2” with a lean build. He enjoys a variety of sports as well as light lifting and cardio to stay in shape. Robin has a straight, light brown hair and green/brown eyes. He has straight white teeth that are almost always showing due to the smile that is constantly on his lips. He keeps his hair a little longer and his face always clean shaven, giving him a boy-next-door look.
Robin is extremely laid back with a southern California mentality. He is fun loving and relaxed with his friends, enjoying things such as surfing, skateboarding and playing guitar. He has a fabulous sense of humor and laughs easily, even if it is at himself. However, he is also a hard worker with a strong work ethic. He is extremely intelligent and works hard to make sure his grades are excellent. We truly enjoy having Robin the program not only because he makes us laugh, but also for the stimulating conversation he offers.
Shopping Cart
No items in cart
Buy ICI/IUI Units
|
IUI Units: 35 vials available |
|
||
|
ICI Units: 0 vials available |
No Current Inventory Please Call for details |
||
|
IUI Units (ART): 3 vials available |
|
||
|
ICI Units (ART): 0 vials available |
No Current Inventory Please Call for details |
||
Extended Info
| Audio Interview | $10.00 | |
|
| Baby Photo | $10.00 | |
|
| Extended Profile | $10.00 | |
|
| Keirsey Test | $10.00 | |
|
| Staff Impression |
|
||
| Genetic Test Results |
|
||
Carrier status
Do you know your carrier status? If not, click on the button below to access the same expanded carrier screening as used by Seattle Sperm Bank! For more information click here.
Get Started