ClinVar Miner

Submissions for variant NM_006206.6(PDGFRA):c.2323+277T>A

gnomAD frequency: 0.72302  dbSNP: rs1388997
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 RCV001685343 SCV001904963 benign not provided 2019-01-10 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001685343 SCV005301840 benign not provided criteria provided, single submitter not provided

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