RS767489236 OCA2

Health Risk Chr 15:28022511
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What This Variant Does
"CLNSIG=4
Associated Conditions
Tyrosinase-positive oculocutaneous albinism
SKIN/HAIR/EYE PIGMENTATION 1
BLUE/NONBLUE EYES
OCA2-related disorder
Inborn genetic diseases
Tyrosinase-positive oculocutaneous albinism
SKIN/HAIR/EYE PIGMENTATION 1
BLUE/NONBLUE EYES
OCA2-related disorder
Inborn genetic diseases
Other Variants in OCA2
rs1555375711 rs387906240 rs74653330 rs121918166 rs121918167 rs387906241 rs121918168 rs121918169 rs121918170 rs755604671
Ask Dr. Hemsworth about this variant