ClinVar Miner

Submissions for variant NM_030928.4(CDT1):c.*6G>C

gnomAD frequency: 0.01684  dbSNP: rs3218723
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
Genetic Services Laboratory, University of Chicago RCV000116635 SCV000150599 benign not specified 2013-04-02 criteria provided, single submitter clinical testing
GeneDx RCV001689644 SCV001914510 benign not provided 2019-02-04 criteria provided, single submitter clinical testing

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