ClinVar Miner

Submissions for variant NM_006206.6(PDGFRA):c.1121+28C>T

gnomAD frequency: 0.17553  dbSNP: rs28489067
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000241697 SCV000311421 benign not specified criteria provided, single submitter clinical testing
GeneDx RCV001636791 SCV001847804 benign not provided 2018-06-23 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001636791 SCV005299646 benign not provided criteria provided, single submitter not provided

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