ClinVar Miner

Submissions for variant NM_007194.4(CHEK2):c.593-9C>T (rs1057517597)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Counsyl RCV000409511 SCV000489286 likely benign Familial cancer of breast 2016-09-12 criteria provided, single submitter clinical testing
Invitae RCV000409511 SCV000757483 likely benign Familial cancer of breast 2017-10-24 criteria provided, single submitter clinical testing

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