ClinVar Miner

Submissions for variant NM_003737.4(DCHS1):c.1467C>A (p.Gly489=)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV003072507 SCV003468175 likely benign not provided 2024-10-17 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV003072507 SCV004811378 uncertain significance not provided 2024-02-01 criteria provided, single submitter clinical testing DCHS1: PM2, BP4

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