RS28940881 TYR
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What This Variant Does
"[OMIM:ALBINISM, OCULAR, AUTOSOMAL RECESSIVE]
Associated Conditions
Oculocutaneous albinism type 1B
Oculocutaneous albinism type 1A
6 conditions
Hypopigmentation of the skin
Iris transillumination defect
Hypopigmentation of hair
Horizontal nystagmus
Albinism
Myopia
Nystagmus
Ocular albinism with congenital sensorineural hearing loss
SKIN/HAIR/EYE PIGMENTATION 3
LIGHT/DARK SKIN
Oculocutaneous albinism
Abnormality of the skin
Other Variants in TYR