ClinVar Miner

Submissions for variant NM_002160.4(TNC):c.637G>A (p.Gly213Ser)

gnomAD frequency: 0.00643  dbSNP: rs7020958
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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 RCV000968648 SCV001116117 benign not provided 2019-12-31 criteria provided, single submitter clinical testing
GeneDx RCV000968648 SCV001863644 benign not provided 2020-01-16 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV002271135 SCV002554943 benign Autosomal dominant nonsyndromic hearing loss 56 2022-03-15 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV000968648 SCV005320646 benign not provided criteria provided, single submitter not provided

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