Variants studied for obsolete Heimler syndrome 2

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	not provided	total
27	81	22	3	10	1	140

Gene and significance breakdown #

Total genes and gene combinations: 1

Download table as spreadsheet

Gene or gene combination	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	not provided	total
PEX6	27	81	22	3	10	1	140

Submitter and significance breakdown #

Total submitters: 12

Download table as spreadsheet

Submitter	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	not provided	total
Baylor Genetics	20	77	5	0	0	0	102
Fulgent Genetics, Fulgent Genetics	1	2	15	3	1	0	22
Genome-Nilou Lab	0	0	1	0	10	0	11
Leeds Amelogenesis Imperfecta Research Group, University of Leeds	7	0	0	0	0	0	7
OMIM	5	0	0	0	0	0	5
Institute of Immunology and Genetics Kaiserslautern	2	0	0	0	0	0	2
Institute of Human Genetics, University of Goettingen	0	1	0	0	0	0	1
Centogene AG - the Rare Disease Company	0	0	1	0	0	0	1
Hadassah Hebrew University Medical Center	0	1	0	0	0	0	1
Institute of Human Genetics, University of Leipzig Medical Center	0	0	1	0	0	0	1
GenomeConnect, ClinGen	0	0	0	0	0	1	1
Service de Biologie Medicale, CIUSSS du Saguenay-Lac-Saint-Jean	0	1	0	0	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.