RS773684789 WFS1
Upload your DNA to see your genotype for this variant.
Associated Conditions
Autosomal dominant nonsyndromic hearing loss 6
Cataract 41
Type 2 diabetes mellitus
Wolfram syndrome 1
Wolfram-like syndrome
WFS1-related disorder
Autosomal dominant nonsyndromic hearing loss 6
Cataract 41
Type 2 diabetes mellitus
Wolfram syndrome 1
Wolfram-like syndrome
WFS1-related disorder
Other Variants in WFS1