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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