ClinVar Miner

Submissions for variant NM_001845.6(COL4A1):c.1962G>A (p.Pro654=)

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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 RCV002511761 SCV002822099 likely benign not provided 2022-10-01 criteria provided, single submitter clinical testing COL4A1: BP4, BP7
Labcorp Genetics (formerly Invitae), Labcorp RCV002511761 SCV003514910 likely benign not provided 2023-01-24 criteria provided, single submitter clinical testing

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