Meet Mason (9869) – Open ID Donor.

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  • Eyes: Blue/Green
  • Hair: Brown
  • Height: 6'01"
  • Weight (lbs): 200
  • Blood: O Rh+
  • CMV: -
  • Ethnicity: Caucasian, French-Canadian, Irish
  • Jewish Ancestry: No
  • Education/Occupation: B.S. Athletic Trainer / Athletic Trainer/Business Owner
  • Live Birth / Pregnancy Confirmed: Yes
  • Extended Testing: Yes
  • Genetically tested for: View

Mason is tall with large muscles, a result of his Olympic lifting. Aside from competitive lifting he also plays hockey and cooks healthy, delicious meals in his free time. He has thick, brown hair that contrasts beautifully with his large, bright blue eyes. Mason has a strong jawline and full lips that frame a constant, broad smile. He normally comes into the office straight from the gym dressed in workout clothes, but he also cleans up nicely in the event of a business meeting dressing in well-fitting business attire. All these features make Mason a uniquely attractive donor.

Mason has a big personality to match the big smile he wears every day. He is extremely outgoing, makes friends wherever he goes and loves to make others smile. He is ambitious and driven to succeed, already on his way as a gym owner. Mason is also thoughtful and reflective, always doing what he can to help others. We believe that Mason would make a wonderful donor 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