Autosomal Dominant Nonsyndromic Hearing Loss 36

Other 50 variants 2 genes

Upload your DNA to see your personal risk score for Autosomal Dominant Nonsyndromic Hearing Loss 36.

Associated Genes (2)
Associated Variants (50)
RSID Gene Risk Allele Odds Ratio Evidence
RS747645756 TMC1 strong
RS200831684 TMC1 strong
RS762248733 TMC1 strong
RS151157872 TMC1 strong
RS79830675 TMC1 strong
RS1057515622 TMC1 strong
RS140398130 TMC1 strong
RS563322370 TMC1 strong
RS775428246 TMC1 strong
RS200171616 TMC1 strong
RS58824091 TMC1 strong
RS191962062 TMC1 strong
RS755694066 TMC1 strong
RS533837914 TMC1 strong
RS2132189585 TMC1 strong
RS764992976 TMC1 strong
RS746724027 TMC1 strong
RS760532554 TMC1 strong
RS1448901281 TMC1 strong
RS2489958072 TMC1 strong
RS2464391981 USH2A strong
RS1355461608 USH2A strong
RS368084452 TMC1 strong
RS772640673 TMC1 strong
RS1289646352 TMC1 strong
RS786201027 TMC1 strong
RS121908073 TMC1 strong
RS151001642 TMC1 strong
RS370898981 TMC1 strong
RS11143384 TMC1 strong
RS370088722 TMC1 strong
RS111033497 TMC1 strong
RS111033265 USH2A strong
RS142073640 TMC1 strong
RS372710475 TMC1 strong
RS145757452 TMC1 strong
RS139985214 TMC1 strong
RS727503485 TMC1 strong
RS121908072 TMC1 strong
RS876658020 TMC1 strong
RS876657727 TMC1 strong
RS138527651 TMC1 strong
RS878853229 TMC1 strong
RS777777359 TMC1 strong
RS113342704 TMC1 strong
RS367924428 TMC1 strong
RS552170649 TMC1 strong
RS150206751 TMC1 strong
RS545955592 TMC1 strong
RS71507808 TMC1 strong
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