Autosomal Dominant Nonsyndromic Hearing Loss 20

Other 61 variants 1 gene

Upload your DNA to see your personal risk score for Autosomal Dominant Nonsyndromic Hearing Loss 20.

Associated Genes (1)
Associated Variants (61)
RSID Gene Risk Allele Odds Ratio Evidence
RS1555666371 ACTG1 strong
RS2143775790 ACTG1 strong
RS2143779222 ACTG1 strong
RS2143775764 ACTG1 strong
RS376850595 ACTG1 strong
RS374907377 ACTG1 strong
RS1367861495 ACTG1 strong
RS2143775617 ACTG1 strong
RS2143778877 ACTG1 strong
RS2143779274 ACTG1 strong
RS2544387148 ACTG1 strong
RS2544392103 ACTG1 strong
RS138240892 ACTG1 strong
RS2031770749 ACTG1 strong
RS2544389679 ACTG1 strong
RS2544392140 ACTG1 strong
RS373618606 ACTG1 strong
RS2544392281 ACTG1 strong
RS2544393285 ACTG1 strong
RS2544392831 ACTG1 strong
RS782818444 ACTG1 strong
RS2544386842 ACTG1 strong
RS543202804 ACTG1 strong
RS2544388195 ACTG1 strong
RS202020778 ACTG1 strong
RS781859294 ACTG1 strong
RS104894544 ACTG1 strong
RS104894545 ACTG1 strong
RS104894546 ACTG1 strong
RS28999112 ACTG1 strong
RS104894547 ACTG1 strong
RS267606630 ACTG1 strong
RS267606631 ACTG1 strong
RS11549190 ACTG1 strong
RS281875327 ACTG1 strong
RS281875328 ACTG1 strong
RS281875329 ACTG1 strong
RS797044730 ACTG1 strong
RS28999111 ACTG1 strong
RS782217473 ACTG1 strong
RS375450454 ACTG1 strong
RS145303691 ACTG1 strong
RS536476533 ACTG1 strong
RS782370155 ACTG1 strong
RS11549191 ACTG1 strong
RS782649322 ACTG1 strong
RS1362994447 ACTG1 strong
RS1598551290 ACTG1 strong
RS1598548614 ACTG1 strong
RS145574149 ACTG1 strong
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