ClinVar Miner

Submissions for variant NM_002160.4(TNC):c.2374G>T (p.Gly792Cys)

gnomAD frequency: 0.00131  dbSNP: rs150868783
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Athena Diagnostics Inc RCV000993337 SCV001146206 benign not provided 2019-04-19 criteria provided, single submitter clinical testing
Institute of Human Genetics, University of Leipzig Medical Center RCV001253304 SCV001428954 uncertain significance Autosomal dominant nonsyndromic hearing loss 56 2016-10-19 criteria provided, single submitter clinical testing
GeneDx RCV000993337 SCV002004493 likely benign not provided 2020-03-24 criteria provided, single submitter clinical testing

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