ClinVar Miner

Submissions for variant NM_007194.4(CHEK2):c.793-9_793-8del

dbSNP: rs1480956379
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Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV003318604 SCV000719677 likely benign not provided 2023-07-21 criteria provided, single submitter clinical testing See Variant Classification Assertion Criteria.
Invitae RCV000636011 SCV000757442 likely benign Familial cancer of breast 2024-01-18 criteria provided, single submitter clinical testing

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