ClinVar Miner

Submissions for variant NM_006206.6(PDGFRA):c.2994C>T (p.Asp998=)

dbSNP: rs1318848523
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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 RCV001460712 SCV001664591 likely benign Gastrointestinal stromal tumor 2023-07-03 criteria provided, single submitter clinical testing

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