RS281865527 TYR

Health Risk Chr 11:89191307
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What This Variant Does
"CLNSIG=5
Associated Conditions
Oculocutaneous albinism type 1A
Inborn genetic diseases
SKIN/HAIR/EYE PIGMENTATION 3
LIGHT/DARK SKIN
TYR-related disorder
Oculocutaneous albinism type 1B
Oculocutaneous albinism type 1A
Inborn genetic diseases
SKIN/HAIR/EYE PIGMENTATION 3
LIGHT/DARK SKIN
TYR-related disorder
Oculocutaneous albinism type 1B
Other Variants in TYR
rs28940876 rs104894314 rs61754388 rs121908011 rs61753185 rs104894313 rs1042602 rs1126809 rs28940877 rs61754393
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