ClinVar Miner

Submissions for variant NM_000251.3(MSH2):c.1662-13T>C

dbSNP: rs1425037913
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV001181994 SCV001347283 likely benign Hereditary cancer-predisposing syndrome 2017-09-26 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002068304 SCV002461622 likely benign Hereditary nonpolyposis colorectal neoplasms 2024-09-08 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV004807367 SCV005429121 likely benign Lynch syndrome 2024-05-14 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV005245746 SCV005896247 likely benign Lynch syndrome 1 2024-12-10 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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