RS121918339 SLC17A8

Health Risk Chr 12:100396373
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What This Variant Does
"[OMIM:?]
Associated Conditions
Autosomal dominant nonsyndromic hearing loss 25
Autosomal dominant nonsyndromic hearing loss 25
Other Variants in SLC17A8
rs373954823 rs201180712 rs138307707 rs140537845 rs11568530 rs141689561 rs374356596 rs141294063 rs748076639 rs2135999616
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