ClinVar Miner

Submissions for variant NM_002160.4(TNC):c.1508G>A (p.Arg503Lys)

gnomAD frequency: 0.00393  dbSNP: rs114407480
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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 RCV000968647 SCV001116116 benign not provided 2019-12-31 criteria provided, single submitter clinical testing
GeneDx RCV000968647 SCV001833488 benign not provided 2020-02-06 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV002271134 SCV002554887 benign Autosomal dominant nonsyndromic hearing loss 56 2022-03-15 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV000968647 SCV005321970 benign not provided criteria provided, single submitter not provided

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