RS1456118236 OCA2

Health Risk Chr 15:28014820
Upload your DNA to see your genotype for this variant.
Associated Conditions
Inborn genetic diseases
Tyrosinase-positive oculocutaneous albinism
Inborn genetic diseases
Tyrosinase-positive oculocutaneous albinism
Other Variants in OCA2
rs1555375711 rs387906240 rs74653330 rs121918166 rs121918167 rs387906241 rs121918168 rs121918169 rs121918170 rs755604671
Ask Dr. Hemsworth about this variant