RS121908927 COCH

Health Risk Chr 14:30877686
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What This Variant Does
"[OMIM:?]
Associated Conditions
Autosomal dominant nonsyndromic hearing loss 9
Autosomal dominant nonsyndromic hearing loss 9
Other Variants in COCH
rs121908928 rs121908929 rs28938175 rs121908930 rs121908932 rs121908934 rs563163157 rs540895576 rs748731866 rs139503327
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