ClinVar Miner

Submissions for variant NM_006206.6(PDGFRA):c.3270A>G (p.Ter1090=)

dbSNP: rs2110359157
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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 RCV001462781 SCV001666707 likely benign Gastrointestinal stromal tumor 2022-12-03 criteria provided, single submitter clinical testing

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