ClinVar Miner

Submissions for variant NM_007194.4(CHEK2):c.1009-18G>A

dbSNP: rs757393834
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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 RCV001179141 SCV001343749 likely benign Hereditary cancer-predisposing syndrome 2018-10-19 criteria provided, single submitter clinical testing
Invitae RCV002559756 SCV003338268 likely benign Familial cancer of breast 2023-12-08 criteria provided, single submitter clinical testing

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