ClinVar Miner

Submissions for variant NM_001080517.3(SETD5):c.3196-64G>A

gnomAD frequency: 0.25205  dbSNP: rs3915844
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 RCV001689190 SCV001913969 benign not provided 2018-07-03 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001689190 SCV005238619 benign not provided criteria provided, single submitter not provided

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