ClinVar Miner

Submissions for variant NM_006206.6(PDGFRA):c.760-7G>T

gnomAD frequency: 0.00001  dbSNP: rs746550287
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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 RCV000465403 SCV000558255 likely benign Gastrointestinal stromal tumor 2024-01-24 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004711124 SCV005257352 likely benign not provided criteria provided, single submitter not provided

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