ClinVar Miner

Submissions for variant NM_006206.6(PDGFRA):c.1221T>C (p.Phe407=)

dbSNP: rs2110280249
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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 RCV001498520 SCV001703270 likely benign Gastrointestinal stromal tumor 2024-01-05 criteria provided, single submitter clinical testing

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