RS727503443 STRC

Health Risk Chr 15:43603362
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What This Variant Does
"CLNSIG=4
Associated Conditions
Rare genetic deafness
Autosomal recessive nonsyndromic hearing loss 16
Rare genetic deafness
Autosomal recessive nonsyndromic hearing loss 16
Other Variants in STRC
rs786200882 rs786200883 rs139956283 rs727503442 rs199839039 rs376104748 rs727505074 rs727503449 rs141749062 rs727503441
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