ClinVar Miner

Submissions for variant NM_006206.6(PDGFRA):c.932-8C>T

gnomAD frequency: 0.00005  dbSNP: rs374863127
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000465639 SCV000558272 likely benign Gastrointestinal stromal tumor 2024-01-28 criteria provided, single submitter clinical testing
Institute for Clinical Genetics, University Hospital TU Dresden, University Hospital TU Dresden RCV003237877 SCV002010537 uncertain significance not provided 2021-11-03 criteria provided, single submitter clinical testing

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