Meet Finnegan (12043) – Anonymous Donor.

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  • Eyes: Brown
  • Hair: Dark Brown
  • Height: 5'05"
  • Weight (lbs): 130
  • Blood: O Rh+
  • CMV: -
  • Ethnicity: Mix, African-American, Norwegian
  • Jewish Ancestry: No
  • Education/Occupation: MA, Museum Studies, Anthropology / Museum Professional
  • Live Birth / Pregnancy Confirmed: Yes
  • Extended Testing: Yes

Finnegan has a small, lean frame, with slender toned muscles and a narrow torso. He has thick, curly black hair, soulful brown eyes, and a smattering of freckles against his smooth, medium skin. He has a small, angular face and an astute and welcoming expression.

Finnegan always speaks very thoughtfully and intelligently; he has a B.A. in Anthropology and a Masters degree in Museum Studies, currently working as a Front Office Manager for a great museum in the Seattle area. Finnegan prides himself on being politically active and being involved in many social issues impacting his local and global communities; we value his adventurous spirit, his strong work ethic, and his kindness. Finnegan is all around 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