RS778909195 STRC

Health Risk Chr 15:43604020
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What This Variant Does
"CLNSIG=4
Associated Conditions
Autosomal recessive nonsyndromic hearing loss 16
Deafness-infertility syndrome
Autosomal recessive nonsyndromic hearing loss 16
Deafness-infertility syndrome
Other Variants in STRC
rs786200882 rs786200883 rs139956283 rs727503442 rs199839039 rs727503443 rs376104748 rs727505074 rs727503449 rs141749062
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