ClinVar Miner

Submissions for variant NM_001080517.3(SETD5):c.1078-310C>G

gnomAD frequency: 0.06586  dbSNP: rs112573190
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 RCV001652863 SCV001866082 benign not provided 2018-09-01 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001652863 SCV005245698 benign not provided criteria provided, single submitter not provided

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