Autosomal Recessive Nonsyndromic Hearing Loss 12

Other 303 variants 1 gene

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Associated Genes (1)
Associated Variants (303)
RSID Gene Risk Allele Odds Ratio Evidence
RS374362883 CDH23 strong
RS111033509 CDH23 strong
RS111033519 CDH23 strong
RS397517323 CDH23 strong
RS80028391 CDH23 strong
RS111033488 CDH23 strong
RS56107171 CDH23 strong
RS149073355 CDH23 strong
RS201610096 CDH23 strong
RS111033453 CDH23 strong
RS41281318 CDH23 strong
RS143136329 CDH23 strong
RS397517329 CDH23 strong
RS77821631 CDH23 strong
RS368377560 CDH23 strong
RS397517333 CDH23 strong
RS56043301 CDH23 strong
RS111033522 CDH23 strong
RS397517334 CDH23 strong
RS143341423 CDH23 strong
RS397517337 CDH23 strong
RS114745089 CDH23 strong
RS376271562 CDH23 strong
RS369513655 CDH23 strong
RS1325941288 CDH23 strong
RS397517309 CDH23 strong
RS121908348 CDH23 strong
RS121908349 CDH23 strong
RS111033271 CDH23 strong
RS121908351 CDH23 strong
RS121908352 CDH23 strong
RS796051861 CDH23 strong
RS121908354 CDH23 strong
RS56216952 CDH23 strong
RS143282422 CDH23 strong
RS141247813 CDH23 strong
RS111033369 CDH23 strong
RS397517307 CDH23 strong
RS111033270 CDH23 strong
RS397517310 CDH23 strong
RS201475055 CDH23 strong
RS200649500 CDH23 strong
RS111033461 CDH23 strong
RS181275139 CDH23 strong
RS188098974 CDH23 strong
RS111033458 CDH23 strong
RS376560330 CDH23 strong
RS143179070 CDH23 strong
RS79805606 CDH23 strong
RS397517321 CDH23 strong
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