ClinVar Miner

Submissions for variant NM_000251.3(MSH2):c.2005+7A>T

dbSNP: rs1573567708
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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 RCV001473806 SCV001677967 likely benign Hereditary nonpolyposis colorectal neoplasms 2022-01-28 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV005249321 SCV005899074 likely benign Lynch syndrome 1 2024-12-11 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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