Autosomal Dominant Nonsyndromic Hearing Loss 2a

Other 33 variants 1 gene

Upload your DNA to see your personal risk score for Autosomal Dominant Nonsyndromic Hearing Loss 2a.

Associated Genes (1)
Associated Variants (33)
RSID Gene Risk Allele Odds Ratio Evidence
RS1648636515 KCNQ4 strong
RS797044969 KCNQ4 strong
RS797044970 KCNQ4 strong
RS797044972 KCNQ4 strong
RS367890569 KCNQ4 strong
RS1271250198 KCNQ4 strong
RS1558014576 KCNQ4 strong
RS374078257 KCNQ4 strong
RS1557977732 KCNQ4 strong
RS797044968 KCNQ4 strong
RS200053059 KCNQ4 strong
RS876657841 KCNQ4 strong
RS373727071 KCNQ4 strong
RS2148319465 KCNQ4 strong
RS2523882381 KCNQ4 strong
RS2523879810 KCNQ4 strong
RS1489698141 KCNQ4 strong
RS28937588 KCNQ4 strong
RS797044967 KCNQ4 strong
RS797044966 KCNQ4 strong
RS797044965 KCNQ4 strong
RS1553165199 KCNQ4 strong
RS137853969 KCNQ4 strong
RS1648206560 KCNQ4 strong
RS80358269 KCNQ4 strong
RS80358273 KCNQ4 strong
RS80358279 KCNQ4 strong
RS80358272 KCNQ4 strong
RS80358276 KCNQ4 strong
RS80358278 KCNQ4 strong
RS80358271 KCNQ4 strong
RS28939710 KCNQ4 strong
RS80358277 KCNQ4 strong
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