Variants in gene SLC11A1

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	risk factor	total
0	0	67	18	9	2	94

Condition and significance breakdown #

Total conditions: 7

Download table as spreadsheet

Condition	uncertain significance	likely benign	benign	risk factor	total
not specified	64	6	0	0	70
not provided	2	7	6	0	15
SLC11A1-related disorder	0	5	4	0	9
Buruli ulcer, susceptibility to	0	0	0	1	1
Cystic fibrosis	1	0	0	0	1
Mycobacterium tuberculosis, susceptibility to	1	0	0	0	1
Mycobacterium tuberculosis, susceptibility to infection by	0	0	0	1	1

Submitter and significance breakdown #

Total submitters: 8

Download table as spreadsheet

Submitter	uncertain significance	likely benign	benign	risk factor	total
Ambry Genetics	64	6	0	0	70
Labcorp Genetics (formerly Invitae), Labcorp	0	5	5	0	10
PreventionGenetics, part of Exact Sciences	0	5	4	0	9
CeGaT Center for Human Genetics Tuebingen	0	2	2	0	4
Department of Pathology and Laboratory Medicine, Sinai Health System	3	0	0	0	3
OMIM	0	0	0	2	2
Breakthrough Genomics, Breakthrough Genomics	0	0	2	0	2
Genomic Research Center, Shahid Beheshti University of Medical Sciences	1	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.