RS61753180 TYR

Health Risk Chr 11:89178093
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What This Variant Does
"[OMIM:?]
Associated Conditions
Oculocutaneous albinism type 1A
Oculocutaneous albinism type 1B
SKIN/HAIR/EYE PIGMENTATION 3
LIGHT/DARK SKIN
Ocular albinism with congenital sensorineural hearing loss
Inborn genetic diseases
TYR-related disorder
Oculocutaneous albinism
Oculocutaneous albinism type 1A
Oculocutaneous albinism type 1B
SKIN/HAIR/EYE PIGMENTATION 3
LIGHT/DARK SKIN
Ocular albinism with congenital sensorineural hearing loss
Inborn genetic diseases
TYR-related disorder
Other Variants in TYR
rs281865527 rs28940876 rs104894314 rs61754388 rs121908011 rs61753185 rs104894313 rs1042602 rs1126809 rs28940877
Ask Dr. Hemsworth about this variant