ClinVar Miner

Submissions for variant NM_006206.6(PDGFRA):c.2661G>A (p.Glu887=)

dbSNP: rs2110341764
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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 RCV001463823 SCV001667771 likely benign Gastrointestinal stromal tumor 2022-07-19 criteria provided, single submitter clinical testing

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