ClinVar Miner

Submissions for variant NM_001080517.3(SETD5):c.1783-30G>A

gnomAD frequency: 0.07310  dbSNP: rs200418836
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 RCV001681990 SCV001902278 benign not provided 2018-09-01 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001681990 SCV005245702 benign not provided criteria provided, single submitter not provided

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