ClinVar Miner

Submissions for variant NM_006206.6(PDGFRA):c.2003-82T>C

gnomAD frequency: 0.95431  dbSNP: rs1907820
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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 RCV001718142 SCV001946238 benign not provided 2018-06-22 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001718142 SCV005301835 benign not provided criteria provided, single submitter not provided

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