Variants studied for sclerosing cholangitis

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		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
16	7	57	65	14	153

Gene and significance breakdown #

Total genes and gene combinations: 4

Download table as spreadsheet

Gene or gene combination	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	total
DCDC2	10	5	51	57	12	129
DCDC2, KAAG1	2	1	6	8	1	18
CLDN1, CLDN16	3	1	0	0	1	5
CLDN1	1	0	0	0	0	1

Submitter and significance breakdown #

Total submitters: 14

Download table as spreadsheet

Submitter	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	total
Labcorp Genetics (formerly Invitae), Labcorp	6	1	52	61	12	132
Fulgent Genetics, Fulgent Genetics	4	2	11	6	0	23
OMIM	8	0	0	0	0	8
Genome-Nilou Lab	0	0	0	0	5	5
University of Washington Center for Mendelian Genomics, University of Washington	2	0	0	0	0	2
3billion	2	0	0	0	0	2
Baylor Genetics	1	0	0	0	0	1
Revvity Omics, Revvity	1	0	0	0	0	1
Centogene AG - the Rare Disease Company	0	1	0	0	0	1
Hadassah Hebrew University Medical Center	0	1	0	0	0	1
Molecular Genetics Department, Kulakov National Medical Research Center for Obstetrics, Gynecology and Perinatology	0	1	0	0	0	1
Human Genetics Section, Sidra Medicine	0	1	0	0	0	1
Pittsburgh Clinical Genomics Laboratory, University of Pittsburgh Medical Center	1	0	0	0	0	1
Neuberg Centre For Genomic Medicine, NCGM	0	0	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.