ClinVar Miner

Submissions for variant NM_007194.4(CHEK2):c.885A>G (p.Glu295=)

dbSNP: rs1555916935
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV001182083 SCV001347433 likely benign Hereditary cancer-predisposing syndrome 2018-11-28 criteria provided, single submitter clinical testing
Invitae RCV001462161 SCV001666074 likely benign Familial cancer of breast 2021-03-26 criteria provided, single submitter clinical testing
Sema4, Sema4 RCV001182083 SCV002537650 uncertain significance Hereditary cancer-predisposing syndrome 2021-11-16 criteria provided, single submitter curation

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