ClinVar Miner

Submissions for variant NM_001287444.2(DCDC2C):c.955-1G>C

gnomAD frequency: 0.00001  dbSNP: rs1167362443
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genomic Medicine Lab, University of California San Francisco RCV001007906 SCV001167614 uncertain significance Cobalamin C disease 2018-10-25 criteria provided, single submitter clinical testing

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