ClinVar Miner

Submissions for variant NM_006206.6(PDGFRA):c.1659G>C (p.Pro553=)

dbSNP: rs150426218
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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 RCV000557699 SCV000630570 likely benign Gastrointestinal stromal tumor 2017-02-28 criteria provided, single submitter clinical testing

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