RS1553879004 WFS1

Health Risk Chr 4:6302184
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Associated Conditions
Rare genetic deafness
Wolfram syndrome 1
WFS1-related disorder
Optic atrophy
Monogenic hearing loss
Autosomal dominant nonsyndromic hearing loss
Rare genetic deafness
Wolfram syndrome 1
WFS1-related disorder
Optic atrophy
Monogenic hearing loss
Autosomal dominant nonsyndromic hearing loss
Other Variants in WFS1
rs28937890 rs28937891 rs104893879 rs28937892 rs1578609780 rs1191510461 rs104893880 rs104893881 rs1362648752 rs28937893
Ask Dr. Hemsworth about this variant