ClinVar Miner

Submissions for variant NM_006206.6(PDGFRA):c.2440-50_2440-49insA

gnomAD frequency: 0.75180  dbSNP: rs3830355
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001696229 SCV001916176 benign not provided 2018-06-22 criteria provided, single submitter clinical testing
Faculté Pluridciplinaire Nador, Université Mohamed Premier RCV001250969 SCV001250952 uncertain significance Squamous cell lung carcinoma 2020-05-05 no assertion criteria provided clinical testing

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