Variants studied for Hemochromatosis type 3

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
15	76	93	34	23	24	230

Gene and significance breakdown #

Total genes and gene combinations: 3

Download table as spreadsheet

Gene or gene combination	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	not provided	total
TFR2	12	62	85	32	23	23	204
LOC113687175, TFR2	3	13	8	2	0	1	25
LOC129998967, TFR2	0	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	not provided	total
Illumina Laboratory Services, Illumina	0	0	68	5	10	0	83
Natera, Inc.	2	3	25	29	17	0	76
Baylor Genetics	8	62	0	0	0	0	70
Fulgent Genetics, Fulgent Genetics	1	20	9	2	0	0	32
GeneReviews	0	0	0	0	0	24	24
Revvity Omics, Revvity	3	3	1	0	0	0	7
OMIM	4	0	0	0	0	0	4
Women's Health and Genetics/Laboratory Corporation of America, LabCorp	1	1	0	0	0	0	2
Genomic Medicine Center of Excellence, King Faisal Specialist Hospital and Research Centre	0	0	2	0	0	0	2
Dept of Medicine and Surgery, University of Milano-Bicocca	2	0	0	0	0	0	2
Genome-Nilou Lab	0	0	1	0	1	0	2
BloodGenetics	0	1	0	0	0	0	1
Victorian Clinical Genetics Services, Murdoch Childrens Research Institute	0	0	1	0	0	0	1
Juno Genomics, Hangzhou Juno Genomics, Inc	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.