RS74315205 WFS1

Health Risk Chr 4:6302385
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What This Variant Does
"[OMIM:WFS1 GENE
Associated Conditions
Wolfram-like syndrome
Autosomal dominant nonsyndromic hearing loss 6
Rare genetic deafness
Wolfram syndrome 1
Nonsyndromic genetic hearing loss
See cases
Retinal dystrophy
Autosomal dominant nonsyndromic hearing loss
Wolfram-like syndrome
Autosomal dominant nonsyndromic hearing loss 6
Rare genetic deafness
Wolfram syndrome 1
Nonsyndromic genetic hearing loss
See cases
Retinal dystrophy
Other Variants in WFS1
rs28937890 rs28937891 rs104893879 rs28937892 rs1578609780 rs1191510461 rs104893880 rs104893881 rs1362648752 rs28937893
Ask Dr. Hemsworth about this variant