Autosomal Dominant Nonsyndromic Hearing Loss 13

Other 39 variants 1 gene

Upload your DNA to see your personal risk score for Autosomal Dominant Nonsyndromic Hearing Loss 13.

Associated Genes (1)
Associated Variants (39)
RSID Gene Risk Allele Odds Ratio Evidence
RS755731113 COL11A2 strong
RS748440351 COL11A2 strong
RS202032297 COL11A2 strong
RS1583335192 COL11A2 strong
RS1259912377 COL11A2 strong
RS1219133025 COL11A2 strong
RS765609390 COL11A2 strong
RS369790491 COL11A2 strong
RS1322629595 COL11A2 strong
RS779116250 COL11A2 strong
RS750173113 COL11A2 strong
RS779998311 COL11A2 strong
RS200635355 COL11A2 strong
RS2534685364 COL11A2 strong
RS763575313 COL11A2 strong
RS2150532832 COL11A2 strong
RS2534810137 COL11A2 strong
RS2534413642 COL11A2 strong
RS764045158 COL11A2 strong
RS2534568745 COL11A2 strong
RS139116571 COL11A2 strong
RS121912948 COL11A2 strong
RS121912950 COL11A2 strong
RS121912951 COL11A2 strong
RS121912952 COL11A2 strong
RS727504460 COL11A2 strong
RS61730262 COL11A2 strong
RS727504458 COL11A2 strong
RS142890313 COL11A2 strong
RS376797260 COL11A2 strong
RS121912947 COL11A2 strong
RS141430703 COL11A2 strong
RS149071920 COL11A2 strong
RS758507327 COL11A2 strong
RS568840295 COL11A2 strong
RS138045609 COL11A2 strong
RS1057524643 COL11A2 strong
RS768569721 COL11A2 strong
RS911722283 COL11A2 strong
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