ClinVar Miner

Submissions for variant NM_006206.6(PDGFRA):c.1599G>A (p.Val533=)

dbSNP: rs146832047
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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 RCV001473445 SCV001677598 likely benign Gastrointestinal stromal tumor 2023-10-16 criteria provided, single submitter clinical testing

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