Nonsyndromic Genetic Hearing Loss

Other 193 variants 14 genes

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Associated Genes (14)
Associated Variants (193)
RSID Gene Risk Allele Odds Ratio Evidence
RS397516335 POU3F4 strong
RS80338940 GJB2 strong
RS104894409 GJB2 strong
RS104894544 ACTG1 strong
RS1801002 GJB2 strong
RS80338949 GJB2 strong
RS80338941 GJB2 strong
RS80356590 OTOF strong
RS80356591 OTOF strong
RS397515435 OTOF strong
RS111033415 MYO7A strong
RS111033290 MYO7A strong
RS111033437 MYO7A strong
RS28931593 GJB2 strong
RS143282422 CDH23 strong
RS111033327 GJB2 strong
RS111033296 GJB2 strong
RS111033293 GJB2 strong
RS111033361 GJB2 strong
RS111033299 GJB2 strong
RS111033253 GJB2 strong
RS397516873 GJB2 strong
RS34988750 GJB2 strong
RS200104362 GJB2 strong
RS1398515998 OTOGL strong
RS104894397 GJB2 strong
RS121908074 TMC1 strong
RS74315205 WFS1 strong
RS121908354 CDH23 strong
RS80356600 OTOF strong
RS80356593 OTOF strong
RS28937588 KCNQ4 strong
RS28938175 COCH strong
RS121908965 MYO15A strong
RS121909062 TECTA strong
RS121909063 TECTA strong
RS35887622 GJB2 strong
RS104894396 GJB2 strong
RS118204027 TRIOBP strong
RS80338939 GJB2 strong
RS104894398 GJB2 strong
RS80338947 GJB2 strong
RS80338950 GJB2 strong
RS80338948 GJB2 strong
RS80338942 GJB2 strong
RS104894402 GJB2 strong
RS80338943 GJB2 strong
RS80338945 GJB2 strong
RS104894401 GJB2 strong
RS72474224 GJB2 strong
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