RS121908929 COCH

Health Risk Chr 14:30878920
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What This Variant Does
"[OMIM:?]
Associated Conditions
Autosomal dominant nonsyndromic hearing loss 9
Hereditary hearing loss and deafness
Autosomal dominant nonsyndromic hearing loss 9
Hereditary hearing loss and deafness
Other Variants in COCH
rs121908927 rs121908928 rs28938175 rs121908930 rs121908932 rs121908934 rs563163157 rs540895576 rs748731866 rs139503327
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