ClinVar Miner

List of variants reported as likely benign for Autosomal recessive nonsyndromic hearing loss 8 by Illumina Laboratory Services, Illumina

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Total variants: 7
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HGVS dbSNP gnomAD frequency
NM_001256317.3(TMPRSS3):c.*409C>T rs55954914 0.05821
NM_001256317.3(TMPRSS3):c.-34G>A rs73372256 0.05210
NM_001256317.3(TMPRSS3):c.268G>A (p.Ala90Thr) rs45598239 0.03352
NM_001256317.3(TMPRSS3):c.432A>G (p.Gln144=) rs61731564 0.02161
NM_001256317.3(TMPRSS3):c.*189T>C rs114813487 0.01262
NM_001256317.3(TMPRSS3):c.*191T>C rs116789917 0.00839
NM_001256317.3(TMPRSS3):c.*246G>A rs57692239 0.00691

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