RS28937893 WFS1

Health Risk Chr 4:6301941
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What This Variant Does
"deafness [OMIM:DEAFNESS, AUTOSOMAL DOMINANT NONSYNDROMIC SENSORINEURAL 6]
Associated Conditions
Autosomal dominant nonsyndromic hearing loss 6
Rare genetic deafness
Monogenic hearing loss
Autosomal dominant nonsyndromic hearing loss 6
Rare genetic deafness
Monogenic hearing loss
Other Variants in WFS1
rs28937890 rs28937891 rs104893879 rs28937892 rs1578609780 rs1191510461 rs104893880 rs104893881 rs1362648752 rs104893883
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