ClinVar Miner

Submissions for variant NM_002609.4(PDGFRB):c.255C>T (p.Leu85=)

gnomAD frequency: 0.00003  dbSNP: rs572557907
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genome Diagnostics Laboratory, Amsterdam University Medical Center RCV001580011 SCV001809365 likely benign not provided no assertion criteria provided clinical testing
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center RCV001580011 SCV001969635 likely benign not provided no assertion criteria provided clinical testing

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