RS797044968 KCNQ4

Health Risk Chr 1:40819461
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What This Variant Does
"CLNSIG=5
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 rs80358279 rs80358273 rs80358269
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