RS876657725 STRC

Health Risk Chr 15:43611237
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What This Variant Does
"CLNSIG=5
Associated Conditions
Rare genetic deafness
Autosomal recessive nonsyndromic hearing loss 16
STRC-related disorder
Rare genetic deafness
Autosomal recessive nonsyndromic hearing loss 16
STRC-related disorder
Other Variants in STRC
rs786200882 rs786200883 rs139956283 rs727503442 rs199839039 rs727503443 rs376104748 rs727505074 rs727503449 rs141749062
Ask Dr. Hemsworth about this variant