ClinVar Miner

Submissions for variant NM_002160.4(TNC):c.3375C>A (p.Ser1125Arg)

dbSNP: rs61737056
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000972461 SCV001120174 benign not provided 2019-12-31 criteria provided, single submitter clinical testing
GeneDx RCV000972461 SCV001901364 benign not provided 2021-04-21 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV002271139 SCV002554427 benign Autosomal dominant nonsyndromic hearing loss 56 2022-03-15 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV000972461 SCV005323151 benign not provided criteria provided, single submitter not provided

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