ClinVar Miner

Submissions for variant NM_000400.4(ERCC2):c.2191-11G>A

dbSNP: rs1568530396
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Institute for Clinical Genetics, University Hospital TU Dresden, University Hospital TU Dresden RCV002540726 SCV002009192 uncertain significance not provided 2021-11-03 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002540726 SCV003202345 likely benign not provided 2023-01-07 criteria provided, single submitter clinical testing

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