ClinVar Miner

Submissions for variant NM_007194.4(CHEK2):c.908+16T>C

dbSNP: rs1198651411
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV001188541 SCV001355614 likely benign Hereditary cancer-predisposing syndrome 2019-07-29 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002560022 SCV003252014 likely benign Familial cancer of breast 2023-12-08 criteria provided, single submitter clinical testing

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