Variants studied for Bartter disease type 4B

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	2	25	21	35	97

Gene and significance breakdown #

Total genes and gene combinations: 4

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Gene or gene combination	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	total
CLCNKB, LOC106501713	10	1	15	19	24	69
CLCNKA, LOC106501712	2	1	6	1	10	20
CLCNKB	2	0	2	1	1	6
CLCNKA	0	0	2	0	0	2

Submitter and significance breakdown #

Total submitters: 8

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Submitter	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	total
Fulgent Genetics, Fulgent Genetics	12	1	17	21	2	53
Genome-Nilou Lab	0	0	0	0	33	33
Genomic Research Center, Shahid Beheshti University of Medical Sciences	0	0	3	0	0	3
OMIM	2	0	0	0	0	2
Baylor Genetics	0	1	1	0	0	2
Revvity Omics, Revvity	0	0	2	0	0	2
Mendelics	0	0	1	0	1	2
Sydney Genome Diagnostics, Children's Hospital Westmead	0	0	1	0	0	1

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