ClinVar Miner

Submissions for variant NM_001378418.1(TCF20):c.4119G>A (p.Ala1373=)

gnomAD frequency: 0.00037  dbSNP: rs533790420
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CeGaT Center for Human Genetics Tuebingen RCV001531982 SCV001747342 likely benign not provided 2021-04-01 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001531982 SCV003253494 benign not provided 2023-12-01 criteria provided, single submitter clinical testing

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