RS146670741 WFS1

Health Risk Chr 4:6301681
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What This Variant Does
"CLNSIG=4
Associated Conditions
Rare genetic deafness
Monogenic diabetes
Inborn genetic diseases
Wolfram syndrome 1
Cataract 41
Wolfram-like syndrome
Autosomal dominant nonsyndromic hearing loss 6
Type 2 diabetes mellitus
Rare genetic deafness
Monogenic diabetes
Inborn genetic diseases
Wolfram syndrome 1
Cataract 41
Wolfram-like syndrome
Autosomal dominant nonsyndromic hearing loss 6
Other Variants in WFS1
rs28937890 rs28937891 rs104893879 rs28937892 rs1578609780 rs1191510461 rs104893880 rs104893881 rs1362648752 rs28937893
Ask Dr. Hemsworth about this variant