RS80358273 KCNQ4

Health Risk Chr 1:40818518
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What This Variant Does
"Identification of novel mutations in the KCNQ4 gene of patients with nonsyndromic deafness from Taiw...
Associated Conditions
Autosomal dominant nonsyndromic hearing loss 2A
KCNQ4-related disorder
Autosomal dominant nonsyndromic hearing loss 2A
KCNQ4-related disorder
Other Variants in KCNQ4
rs28937588 rs80358277 rs28939710 rs80358271 rs80358278 rs80358276 rs80358272 rs80358279 rs80358269 rs1648206560
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