ClinVar Miner

Submissions for variant NM_006206.6(PDGFRA):c.3018T>G (p.Gly1006=)

dbSNP: rs1207081282
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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 RCV001464549 SCV001668522 likely benign Gastrointestinal stromal tumor 2019-01-25 criteria provided, single submitter clinical testing

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