RS200053059 KCNQ4

Health Risk Chr 1:40818177
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Associated Conditions
Hearing impairment
Inborn genetic diseases
Autosomal dominant nonsyndromic hearing loss 2A
Hearing impairment
Inborn genetic diseases
Autosomal dominant nonsyndromic hearing loss 2A
Other Variants in KCNQ4
rs28937588 rs80358277 rs28939710 rs80358271 rs80358278 rs80358276 rs80358272 rs80358279 rs80358273 rs80358269
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