Meet Vince (9918) – Open ID Donor.

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Vince stands at 6 feet tall with broad shoulders and a good build. Vince keeps active and in shape by playing recreational sports along with some light weightlifting and regular cardiovascular activity. He has a clear, smooth complexion that tans when he spends time in the sun and symmetrical facial features. Vince has amazing thick, wavy brown hair that makes his bright green/blue eyes pop. All these features work together to make Vince an exceptionally handsome donor.


Aside from his good looks, Vince is also incredibly thoughtful and intelligent. He is currently pursuing a Master of Science in Psychology and achieved a nearly 4.0 GPA in his undergraduate degree. He is an avid reader and always looking to learn something new; currently Vince is teaching himself how to play the guitar. Vince comes from a very close family that he is extremely proud to be a part of. When asked why he wants to be a donor, Vince answered, “I want to be a donor because I know that there are people that want to start a family of their own but are unable to due to a variety of circumstances, and I am in a position to help with that.” Vince has both intelligence and good looks and would make a great 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