RS200135768 WFS1

Health Risk Chr 4:6277682
Upload your DNA to see your genotype for this variant.
Associated Conditions
Monogenic diabetes
WFS1-Related Spectrum Disorders
Autosomal dominant nonsyndromic hearing loss 6
Wolfram syndrome 1
Inborn genetic diseases
WFS1-related disorder
Monogenic diabetes
WFS1-Related Spectrum Disorders
Autosomal dominant nonsyndromic hearing loss 6
Wolfram syndrome 1
Inborn genetic diseases
WFS1-related disorder
Other Variants in WFS1
rs28937890 rs28937891 rs104893879 rs28937892 rs1578609780 rs1191510461 rs104893880 rs104893881 rs1362648752 rs28937893
Ask Dr. Hemsworth about this variant