ClinVar Miner

Submissions for variant NM_000251.3(MSH2):c.211+10G>C

dbSNP: rs2103883273
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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 RCV001461828 SCV001665737 likely benign Hereditary nonpolyposis colorectal neoplasms 2019-02-28 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV005247112 SCV005895115 likely benign Lynch syndrome 1 2024-12-03 criteria provided, single submitter clinical testing This variant is considered likely benign. This variant is intronic and is not expected to impact mRNA splicing.

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