RS80358271 KCNQ4

Health Risk Chr 1:40784304
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What This Variant Does
"Mutations in the KCNQ4 gene are responsible for autosomal dominant deafness in four DFNA2 families. ...
Associated Conditions
Autosomal dominant nonsyndromic hearing loss 2A
Autosomal dominant nonsyndromic hearing loss 2A
Other Variants in KCNQ4
rs28937588 rs80358277 rs28939710 rs80358278 rs80358276 rs80358272 rs80358279 rs80358273 rs80358269 rs1648206560
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