RS121908011 TYR
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What This Variant Does
"[OMIM:?]
Associated Conditions
Oculocutaneous albinism type 1A
Oculocutaneous albinism type 1B
Nonsyndromic Oculocutaneous Albinism
Ocular albinism with congenital sensorineural hearing loss
SKIN/HAIR/EYE PIGMENTATION 3
LIGHT/DARK SKIN
Inborn genetic diseases
Oculocutaneous albinism
TYR-related disorder
Oculocutaneous albinism type 1A
Oculocutaneous albinism type 1B
Nonsyndromic Oculocutaneous Albinism
Ocular albinism with congenital sensorineural hearing loss
SKIN/HAIR/EYE PIGMENTATION 3
LIGHT/DARK SKIN
Other Variants in TYR