RS104894414 GJB6

Health Risk Chr 13:20223467
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What This Variant Does
"[OMIM:?]
Associated Conditions
Autosomal dominant nonsyndromic hearing loss 3B
Autosomal dominant nonsyndromic hearing loss 3B
Other Variants in GJB6
rs778513540 rs2137333664 rs2137333887 rs1869351345 rs200172266 rs377181573 rs772862268 rs1566538321 rs543659673 rs145438428
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