Autosomal Recessive Nonsyndromic Hearing Loss 31

Other 49 variants 1 gene

Upload your DNA to see your personal risk score for Autosomal Recessive Nonsyndromic Hearing Loss 31.

Associated Genes (1)
Associated Variants (49)
RSID Gene Risk Allele Odds Ratio Evidence
RS1064794551 WHRN strong
RS760471578 WHRN strong
RS141807746 WHRN strong
RS147500559 WHRN strong
RS569159249 WHRN strong
RS547616329 WHRN strong
RS201105262 WHRN strong
RS779112096 WHRN strong
RS549195233 WHRN strong
RS781674400 WHRN strong
RS150407952 WHRN strong
RS147477922 WHRN strong
RS758129253 WHRN strong
RS143443833 WHRN strong
RS556585167 WHRN strong
RS776268964 WHRN strong
RS372472927 WHRN strong
RS143763650 WHRN strong
RS529176890 WHRN strong
RS143728180 WHRN strong
RS748769354 WHRN strong
RS201171374 WHRN strong
RS377363590 WHRN strong
RS763014940 WHRN strong
RS145985595 WHRN strong
RS45527543 WHRN strong
RS56059137 WHRN strong
RS149558159 WHRN strong
RS200377723 WHRN strong
RS111033459 WHRN strong
RS79572315 WHRN strong
RS139337135 WHRN strong
RS146655362 WHRN strong
RS35258467 WHRN strong
RS56204273 WHRN strong
RS201555289 WHRN strong
RS61743618 WHRN strong
RS137852839 WHRN strong
RS76593842 WHRN strong
RS146273185 WHRN strong
RS150586098 WHRN strong
RS142568702 WHRN strong
RS187221008 WHRN strong
RS572671060 WHRN strong
RS200131193 WHRN strong
RS779760634 WHRN strong
RS142653982 WHRN strong
RS869320674 WHRN strong
RS55966714 WHRN strong
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