ClinVar Miner

Submissions for variant NM_006206.6(PDGFRA):c.1920T>C (p.Ala640=)

dbSNP: rs2110311129
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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 RCV001406772 SCV001608728 likely benign Gastrointestinal stromal tumor 2020-10-23 criteria provided, single submitter clinical testing

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