ClinVar Miner

Submissions for variant NM_002609.4(PDGFRB):c.2549A>G (p.Asp850Gly)

dbSNP: rs1060499540
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Revvity Omics, Revvity RCV003131894 SCV003814805 uncertain significance not provided 2022-08-24 criteria provided, single submitter clinical testing
Genomic Medicine Center of Excellence, King Faisal Specialist Hospital and Research Centre RCV003989818 SCV004807045 uncertain significance Myofibromatosis, infantile, 1 2024-03-26 criteria provided, single submitter clinical testing

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