ClinVar Miner

Submissions for variant NM_002907.4(RECQL):c.701-4del

dbSNP: rs1424768811
Minimum review status: Collection method:
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 RCV000842198 SCV000984197 likely benign not provided 2023-10-31 criteria provided, single submitter clinical testing See Variant Classification Assertion Criteria.
Labcorp Genetics (formerly Invitae), Labcorp RCV000842198 SCV001732074 benign not provided 2023-12-22 criteria provided, single submitter clinical testing

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