Autosomal Dominant Nonsyndromic Hearing Loss 44

Other 2 variants 1 gene

Upload your DNA to see your personal risk score for Autosomal Dominant Nonsyndromic Hearing Loss 44.

Associated Genes (1)
CCDC50
Associated Variants (2)
RSID Gene Risk Allele Odds Ratio Evidence
RS2108677025 CCDC50 — — strong
RS138443787 CCDC50 — — strong
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