RS104894313 TYR
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What This Variant Does
"[OMIM:?]
Associated Conditions
Oculocutaneous albinism type 1B
Oculocutaneous albinism
Oculocutaneous albinism type 1A
Inborn genetic diseases
SKIN/HAIR/EYE PIGMENTATION 3
LIGHT/DARK SKIN
Ocular albinism with congenital sensorineural hearing loss
Hearing impairment
Abnormality of the skin
TYR-related disorder
Albinism or congenital nystagmus
Autosomal recessive TYR-related disorders
Pigmentary skin disorders
Oculocutaneous albinism type 1B
Oculocutaneous albinism
Other Variants in TYR