Meet Allister (9993) – Open ID Donor.

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  • Eyes: Blue
  • Hair: Blonde
  • Height: 5'10"
  • Weight (lbs): 135
  • Blood: O Rh+
  • CMV: -
  • Ethnicity: Caucasian, French, German, Irish, Norwegian
  • Jewish Ancestry: No
  • Education/Occupation: B.A. Finance & Accounting / Operations Analyst
  • Live Birth / Pregnancy Confirmed: No
  • Extended Testing: Yes

Allister has very sharp, angular facial features including prominent cheek bones and a strong jaw line. He has well-defined muscles that are long and lean and he stays fit with regular cardio and weight lifting. He is very athletic and grew up playing in a variety of sports, still participating today in many sports at a recreational level. Allister has dark blue eyes and straight blonde hair with a medium skin tone. He has a smooth complexion that he keeps clean shaven for a very clean cut look, making him an attractive young man.

Allister is confident and outgoing, making friends easily in any situation. He is a strong leader but always looks to lighten the situation by making people smile. Allister is driven and smart, setting goals for himself and doing his best to achieve them. His ambition and drive coupled with his athletic ability make Allister a great donor.

Genetic Testing

Over the years, we have expanded our 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. All donors have undergone genetic testing for Cystic Fibrosis, Spinal Muscular Atrophy and Karyotyping.  However, many donors have had more extensive testing performed.

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 contact us, and we will provide a copy of the donor's test reports to your physician and/or genetic counselor.

Karyotyping  Normal Male Karyoptype, 46XY
ABCC8-related hyperinsulinism Non-Carrier
alpha thalassemia Non-Carrier
ARSACS Non-Carrier
Bloom syndrome Non-Carrier
Canavan disease Non-Carrier
cystic fibrosis Non-Carrier
familial dysautonomia Non-Carrier
Fanconi anemia type C Non-Carrier
Gaucher disease Non-Carrier
glycogen storage disease type Ia Non-Carrier
Hb beta chain-related hemoglobinopathy (including beta thalassemia and sickle cell disease) No disease-causing mutations detected; normal complete blood count and hemoglobin analysis
hexosaminidase A deficiency (including Tay-Sachs disease) Non-Carrier
Joubert syndrome 2 Non-Carrier
lipoamide dehydrogenase deficiency Non-Carrier
maple syrup urine disease type 1B Non-Carrier
mucolipidosis IV Non-Carrier
NEB-related nemaline myopathy Non-Carrier
Niemann-Pick disease, SMPD1-associated Non-Carrier
spinal muscular atrophy No disease-causing mutations detected (2 copies or more)
Usher syndrome type 1F Non-Carrier
Usher syndrome type 3 Non-Carrier
Walker-Warburg syndrome Non-Carrier