Variants studied for acrodermatitis enteropathica

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
14	8	94	37	29	164

Gene and significance breakdown #

Total genes and gene combinations: 2

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Gene or gene combination	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	total
SLC39A4	14	8	90	37	29	160
LOC130001397, SLC39A4	0	0	4	0	0	4

Submitter and significance breakdown #

Total submitters: 12

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Submitter	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	total
Natera, Inc.	1	1	32	27	23	84
Illumina Laboratory Services, Illumina	0	0	62	11	10	83
OMIM	12	0	0	0	0	12
Genome-Nilou Lab	0	0	1	1	10	12
Fulgent Genetics, Fulgent Genetics	0	5	2	3	1	11
Revvity Omics, Revvity	0	2	1	0	0	3
Women's Health and Genetics/Laboratory Corporation of America, LabCorp	2	0	0	0	0	2
Baylor Genetics	0	0	1	0	0	1
Institute of Human Genetics, University of Leipzig Medical Center	0	0	1	0	0	1
SIB Swiss Institute of Bioinformatics	0	0	0	0	1	1
Pars Genome Lab	0	0	0	0	1	1
Clinical Laboratory Sciences Program (CLSP), King Saud bin Abdulaziz University for Health Sciences (KSAU-HS)	0	0	1	0	0	1

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