RS80358279 KCNQ4

Health Risk Chr 1:40819926
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What This Variant Does
"A novel KCNQ4 pore-region mutation (p.G296S) causes deafness by impairing cell-surface channel expre...
Associated Conditions
Autosomal dominant nonsyndromic hearing loss 2A
Autosomal dominant nonsyndromic hearing loss 2A
Other Variants in KCNQ4
rs28937588 rs80358277 rs28939710 rs80358271 rs80358278 rs80358276 rs80358272 rs80358273 rs80358269 rs1648206560
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