ClinVar Miner

Submissions for variant NM_000179.3(MSH6):c.3438+6T>C

gnomAD frequency: 0.00001  dbSNP: rs370170322
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001703972 SCV000515856 likely benign not provided 2020-10-14 criteria provided, single submitter clinical testing This variant is associated with the following publications: (PMID: 28531214)
Labcorp Genetics (formerly Invitae), Labcorp RCV000546237 SCV000624865 likely benign Hereditary nonpolyposis colorectal neoplasms 2024-12-17 criteria provided, single submitter clinical testing
Color Diagnostics, LLC DBA Color Health RCV000774608 SCV000908419 likely benign Hereditary cancer-predisposing syndrome 2016-11-10 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV004804042 SCV005424958 likely benign Lynch syndrome 2024-08-13 criteria provided, single submitter clinical testing

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