ClinVar Miner

Submissions for variant NM_006206.6(PDGFRA):c.759+18G>A

gnomAD frequency: 0.00006  dbSNP: rs777100767
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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 RCV002217486 SCV002365828 likely benign Gastrointestinal stromal tumor 2024-01-27 criteria provided, single submitter clinical testing

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