ClinVar Miner

Submissions for variant NM_002160.4(TNC):c.3353G>A (p.Arg1118Gln)

gnomAD frequency: 0.01534  dbSNP: rs61738263
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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000965795 SCV001113072 benign not provided 2019-12-31 criteria provided, single submitter clinical testing
GeneDx RCV000965795 SCV001895600 benign not provided 2019-01-02 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV002271131 SCV002554438 benign Autosomal dominant nonsyndromic hearing loss 56 2022-03-15 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002271131 SCV002810215 likely benign Autosomal dominant nonsyndromic hearing loss 56 2021-08-17 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV000965795 SCV005323263 benign not provided criteria provided, single submitter not provided

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