ClinVar Miner

Variants studied for Interstitial nephritis, karyomegalic

Coded as:
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:

If a variant has more than one submission, it may be counted in more than one significance column. If this is the case, the total number of variants will be less than the sum of the other cells.

pathogenic likely pathogenic uncertain significance likely benign benign total
10 1 2 0 0 13

Gene and significance breakdown #

Total genes and gene combinations: 2
Download table as spreadsheet
Gene or gene combination pathogenic likely pathogenic uncertain significance total
FAN1, MTMR10 6 1 0 7
FAN1 4 0 2 6

Submitter and significance breakdown #

Total submitters: 6
Download table as spreadsheet
Submitter pathogenic likely pathogenic uncertain significance total
OMIM 8 0 0 8
Victorian Clinical Genetics Services,Murdoch Childrens Research Institute 1 1 0 2
Center of Genomic medicine, Geneva,University Hospital of Geneva 2 0 0 2
Fulgent Genetics,Fulgent Genetics 0 0 1 1
Center for Precision Medicine,Vanderbilt University Medical Center 0 0 1 1
UOSD Laboratory of Genetics & Genomics of Rare Diseases,Istituto Giannina Gaslini 1 0 0 1

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.