ClinVar Miner

Submissions for variant NM_006206.6(PDGFRA):c.2003-116A>C

gnomAD frequency: 0.43888  dbSNP: rs4493602
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 RCV001680630 SCV001898341 benign not provided 2019-08-19 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001680630 SCV005301833 benign not provided criteria provided, single submitter not provided

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