ClinVar Miner

Submissions for variant NM_007194.4(CHEK2):c.1543-10T>C

dbSNP: rs1555911654
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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 RCV000771656 SCV000904280 likely benign Hereditary cancer-predisposing syndrome 2017-10-08 criteria provided, single submitter clinical testing
Invitae RCV001394120 SCV001595802 likely benign Familial cancer of breast 2023-04-19 criteria provided, single submitter clinical testing

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