ClinVar Miner

Submissions for variant NM_000251.3(MSH2):c.2635-11A>G

gnomAD frequency: 0.00002  dbSNP: rs201291595
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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV000583741 SCV000690085 likely benign Hereditary cancer-predisposing syndrome 2016-01-04 criteria provided, single submitter clinical testing
GeneDx RCV001683596 SCV001902123 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002061842 SCV002351675 likely benign Hereditary nonpolyposis colorectal neoplasms 2024-02-01 criteria provided, single submitter clinical testing
Sema4, Sema4 RCV000583741 SCV002534494 uncertain significance Hereditary cancer-predisposing syndrome 2021-09-18 criteria provided, single submitter curation
Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital RCV003320710 SCV004024769 likely benign not specified 2023-08-15 criteria provided, single submitter clinical testing

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