ClinVar Miner

Submissions for variant NM_007194.4(CHEK2):c.683+10T>C (rs747427230)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000458706 SCV000560997 likely benign Familial cancer of breast 2016-10-11 criteria provided, single submitter clinical testing
Color RCV000580978 SCV000684677 likely benign Hereditary cancer-predisposing syndrome 2017-03-09 criteria provided, single submitter clinical testing

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