Meet Jeb (12020) – Open ID Donor.

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Jeb Staff Impression

Jeb has thick, wavy, light brown hair, blue/green eyes, and a medium complexion with olive undertones that tans very dark in the summer, which he accredits to his Italian heritage. He has a lean, medium build and is very athletic. Jeb’s face is all around incredibly handsome- he has a square jawline, great cheekbones, large eyes, and a large, friendly smile.

Jeb had a very successful collegiate career, graduating with a double major in Business Management and Marketing. Not surprisingly, he has been working his way up the corporate ladder, now serving as a Regional Manager for a major beverage distributor.  Jeb is a huge food and wine enthusiast; some of his other hobbies include wakeboarding, hunting, fishing, and traveling in general. He also comes from a long line of athletes- both his father and his two brothers played college football, and Jeb also participated in football, wrestling, golf, and tennis before becoming more involved in academics. Jeb is a friendly, charismatic, and smart guy, and makes an amazing 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