ClinVar Miner

Submissions for variant NM_004608.4(TBX6):c.408C>T (p.Arg136=)

gnomAD frequency: 0.00102  dbSNP: rs149724027
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000326250 SCV000341611 uncertain significance not provided 2016-05-13 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000326250 SCV001032104 benign not provided 2023-12-14 criteria provided, single submitter clinical testing

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