ClinVar Miner

Submissions for variant NM_000251.3(MSH2):c.1076+10T>C

dbSNP: rs1558466828
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV000777037 SCV000912718 likely benign Hereditary cancer-predisposing syndrome 2017-12-11 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002067351 SCV002361290 likely benign Hereditary nonpolyposis colorectal neoplasms 2024-04-29 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV005249068 SCV005897529 likely benign Lynch syndrome 1 2024-12-06 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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