ClinVar Miner

Submissions for variant NM_006206.6(PDGFRA):c.189A>G (p.Glu63=)

gnomAD frequency: 0.00002  dbSNP: rs753972328
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001471030 SCV001675132 likely benign Gastrointestinal stromal tumor 2020-03-23 criteria provided, single submitter clinical testing

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