Meet Yale (12027) – Open ID Donor – New Donor!.

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  • Eyes: Brown
  • Hair: Brown
  • Height: 6'00"
  • Weight (lbs): 180
  • Blood: A Rh+
  • CMV: -
  • Ethnicity: Caucasian, German, Scottish
  • Jewish Ancestry: No
  • Education/Occupation: BS Engineering / Design Engineer
  • Live Birth / Pregnancy Confirmed: No
  • Extended Testing: Yes

Yale has a long, lean build with a slender torso, strong shoulders and arms, and long legs. His face is very happy and expressive- he has a square face, a long slender nose, a dominant brow, and a large, cheerful smile. He has a medium skin tone with light olive undertones and rosy cheeks. He has short, thick dark brown hair and dark eyebrows. Overall, his features are very attractive!

Yale is a very smart, dedicated, and hard-working young guy. He excelled academically in high school and college, and has been working his way up the ladder as a Mechanical Engineer for an aerospace company, which he hopes to continue doing for many years. He is a family man, and chats often with the staff about his adorable daughter, whom he takes a lot of pride in. His hobbies are pretty typical of your Pacific Northwestern man- he loves hiking, camping, snowboarding, and off-roading. Yale is all around a super nice, intelligent, and motivated guy, and we think he’d be a great choice for any family!

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