RS71524377 WFS1
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
WFS1-Related Spectrum Disorders
Autosomal dominant nonsyndromic hearing loss 6
Wolfram syndrome 1
Wolfram-like syndrome
Cataract 41
Type 2 diabetes mellitus
WFS1-Related Spectrum Disorders
Autosomal dominant nonsyndromic hearing loss 6
Wolfram syndrome 1
Wolfram-like syndrome
Cataract 41
Type 2 diabetes mellitus
Other Variants in WFS1