ClinVar Miner

Submissions for variant NM_007194.4(CHEK2):c.793-17T>G

dbSNP: rs778511901
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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 RCV001185486 SCV001351706 likely benign Hereditary cancer-predisposing syndrome 2019-10-14 criteria provided, single submitter clinical testing
Invitae RCV002559908 SCV003450150 likely benign Familial cancer of breast 2022-09-06 criteria provided, single submitter clinical testing

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