ClinVar Miner

Submissions for variant NM_002608.4(PDGFB):c.657C>A (p.Pro219=)

gnomAD frequency: 0.01663  dbSNP: rs35978693
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000958221 SCV001105050 benign not provided 2025-01-29 criteria provided, single submitter clinical testing
GeneDx RCV000958221 SCV001898735 benign not provided 2019-06-01 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV000958221 SCV005278753 benign not provided criteria provided, single submitter not provided

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