Autosomal Dominant Nonsyndromic Hearing Loss 22

Other 84 variants 2 genes

Upload your DNA to see your personal risk score for Autosomal Dominant Nonsyndromic Hearing Loss 22.

Associated Genes (2)
Associated Variants (84)
RSID Gene Risk Allele Odds Ratio Evidence
RS541767003 MYO6 strong
RS758630450 MYO6 strong
RS375754710 MYO6 strong
RS752948085 MYO6 strong
RS529167250 MYO6 strong
RS139174622 MYO6 strong
RS571307356 MYO6 strong
RS116215208 MYO6 strong
RS146133231 MYO6 strong
RS570884031 MYO6 strong
RS189155544 MYO6 strong
RS540365866 MYO6 strong
RS118121148 MYO6 strong
RS768643110 MYO6 strong
RS148227849 MYO6 strong
RS188959117 MYO6 strong
RS765929647 MYO6 strong
RS1775958137 MYO6 strong
RS1777874560 MYO6 strong
RS749752357 MYO6 strong
RS2535553134 MYO6 strong
RS2535544061 MYO6 strong
RS2534950585 MYO6 strong
RS2535543931 MYO6 strong
RS2535265747 MYO6 strong
RS187631847 MYO6 strong
RS145665265 MYO6 strong
RS144038082 MYO6 strong
RS727504567 MYO6 strong
RS565770950 MYO6 strong
RS6925845 MYO6 strong
RS150876010 MYO6 strong
RS138437852 MYO6 strong
RS886061759 MYO6 strong
RS146682372 MYO6 strong
RS750374337 MYO6 strong
RS188719640 MYO6 strong
RS147347025 MYO6 strong
RS114970874 MYO6 strong
RS188568413 MYO6 strong
RS79815348 MYO6 strong
RS9443200 MYO6 strong
RS185154265 MYO6 strong
RS570588843 MYO6 strong
RS1060499799 MYO6 strong
RS776737413 BIN1 strong
RS551348450 MYO6 strong
RS1554218566 MYO6 strong
RS766700803 MYO6 strong
RS1582024232 MYO6 strong
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