ClinVar Miner

Submissions for variant NM_006206.6(PDGFRA):c.1233T>C (p.Thr411=)

dbSNP: rs2110280356
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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 RCV002200580 SCV002484336 likely benign Gastrointestinal stromal tumor 2020-12-20 criteria provided, single submitter clinical testing

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