RS387907149 CEACAM16

Health Risk Chr 19:44704053
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What This Variant Does
"CLNSIG=5
Associated Conditions
Autosomal dominant nonsyndromic hearing loss 4B
Autosomal dominant nonsyndromic hearing loss 4B
Other Variants in CEACAM16
rs200297676 rs755154488 rs876661405 rs746164064 rs61729706 rs367891074 rs746541677 rs373050209 rs375722926 rs1568528171
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