ClinVar Miner

Submissions for variant NM_000110.4(DPYD):c.851-31C>T

gnomAD frequency: 0.01754  dbSNP: rs2786491
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
GeneDx RCV000086492 SCV001836935 benign not provided 2018-07-05 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV000086492 SCV005281614 benign not provided criteria provided, single submitter not provided
Diasio Lab, Mayo Clinic RCV000086492 SCV000118658 not provided not provided no assertion provided not provided

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