ClinVar Miner

Submissions for variant NM_006206.6(PDGFRA):c.966C>T (p.Ser322=)

dbSNP: rs1350863455
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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 RCV001502003 SCV001706825 likely benign Gastrointestinal stromal tumor 2021-12-27 criteria provided, single submitter clinical testing

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