RS121912618 WFS1
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What This Variant Does
"[OMIM:?]
Associated Conditions
Autosomal dominant nonsyndromic hearing loss 6
Wolfram syndrome 1
Cataract 41
Wolfram-like syndrome
Type 2 diabetes mellitus
WFS1-related disorder
Optic atrophy
Autosomal dominant nonsyndromic hearing loss 6
Wolfram syndrome 1
Cataract 41
Wolfram-like syndrome
Type 2 diabetes mellitus
WFS1-related disorder
Optic atrophy
Other Variants in WFS1