ClinVar Miner

Submissions for variant NM_007194.4(CHEK2):c.845_846+36dup

dbSNP: rs1064794357
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001704611 SCV000568939 likely benign not provided 2018-10-09 criteria provided, single submitter clinical testing This variant is associated with the following publications: (PMID: 29649263)

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