RS61754381 TYR
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What This Variant Does
"CLNSIG=5
Associated Conditions
Oculocutaneous albinism type 1A
Oculocutaneous albinism
Albinism
Nystagmus
Myopia
Oculocutaneous albinism type 1B
Nonsyndromic Oculocutaneous Albinism
Abnormality of the skin
SKIN/HAIR/EYE PIGMENTATION 3
LIGHT/DARK SKIN
See cases
TYR-related disorder
Albinism or congenital nystagmus
Inborn genetic diseases
Oculocutaneous albinism type 1A
Other Variants in TYR