ClinVar Miner

Submissions for variant NM_001080517.3(SETD5):c.811-225del

dbSNP: rs375612987
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001530849 SCV001745752 benign not provided 2019-09-22 criteria provided, single submitter clinical testing

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