ClinVar Miner

Submissions for variant NM_002160.4(TNC):c.4740C>T (p.Thr1580=)

gnomAD frequency: 0.00277  dbSNP: rs146504512
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ClinVar version:
Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000963498 SCV001110659 benign not provided 2019-12-31 criteria provided, single submitter clinical testing
GeneDx RCV000963498 SCV001851095 benign not provided 2020-03-05 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV002271129 SCV002554405 benign Autosomal dominant nonsyndromic hearing loss 56 2022-03-15 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV000963498 SCV005320937 benign not provided criteria provided, single submitter not provided

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