Meet Nixon (12049) – Open ID Donor.

Back to Donor Search
  • Eyes: Blue
  • Hair: Blonde
  • Height: 6'01"
  • Weight (lbs): 210
  • Blood: A Rh+
  • CMV: -
  • Ethnicity: Caucasian, German
  • Jewish Ancestry: No
  • Education/Occupation: B.A. Political Science / Student
  • Live Birth / Pregnancy Confirmed: Yes
  • Extended Testing: Yes
  • Genetically tested for: View

Nixon has an athletic build, with broad shoulders and strong arms. He has a medium skin tone that tans dark in the summer, wavy dark blonde hair, sparkling blue eyes, a rounded face, and full lips. Overall, he is very attractive and presents himself very well!

Nixon always has a great attitude- he is fun, laid-back, quirky, and to the point. He is currently finishing his degree in Political Economics, with a goal to soon get into one of my many prominent tech sales companies in the Pacific Northwest. He definitely has the charisma and the knack for business and numbers needed to go very far in his desired profession. In his personal time, Nixon is an avid cook, loves to eat, hike, and ski; he is also very active in wrestling, which he has done since high school and still does collegiately. If you are looking for someone direct, confident, and fun-loving, Nixon would be a great choice for you!

 

 

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