ClinVar Miner

Variants with conflicting interpretations "likely pathogenic" from Cancer Genomics Group, Japanese Foundation For Cancer Research and "pathogenic" from any submitter

Minimum review status of the submission from Cancer Genomics Group, Japanese Foundation For Cancer Research: Collection method of the submission from Cancer Genomics Group, Japanese Foundation For Cancer Research:
Minimum review status of the other submission: Collection method of the other submission:
ClinVar version:
Total variants with conflicting interpretations: 1
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_002878.4(RAD51D):c.270_271dup (p.Lys91fs) rs753862052

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.