ClinVar Miner

Submissions for variant NM_007194.4(CHEK2):c.444+7_444+8insTCTCCTAG

dbSNP: rs1555927106
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000560435 SCV000633189 likely benign Familial cancer of breast 2017-03-07 criteria provided, single submitter clinical testing

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