ClinVar Miner

Submissions for variant NM_000110.4(DPYD):c.2908-69A>G

gnomAD frequency: 0.79607  dbSNP: rs290855
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
GeneDx RCV001598463 SCV001831776 benign not provided 2018-07-09 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001598463 SCV005281597 benign not provided criteria provided, single submitter not provided

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