Variants studied for Congenital secretory sodium diarrhea 8

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
11	5	5	4	9	32

Gene and significance breakdown #

Total genes and gene combinations: 1

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Gene or gene combination	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	total
SLC9A3	11	5	5	4	9	32

Submitter and significance breakdown #

Total submitters: 11

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Submitter	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	total
Genome-Nilou Lab	0	0	0	0	9	9
OMIM	8	0	0	0	0	8
Aleixo Muise Laboratory, Hospital For Sick Children	6	2	0	0	0	8
Revvity Omics, Revvity	0	0	2	1	0	3
3billion, Medical Genetics	0	0	0	3	0	3
Baylor Genetics	0	0	1	0	0	1
Mayo Clinic Laboratories, Mayo Clinic	0	0	1	0	0	1
Biochemical Molecular Genetic Laboratory, King Abdulaziz Medical City	0	1	0	0	0	1
Medical Genetics Department, Assistance Publique Hopitaux de Marseille	0	1	0	0	0	1
New York Genome Center	0	0	1	0	0	1
Medical Genetics Department, Ankara Oncology Training and Research Hospital, University of Health Sciences	0	1	0	0	0	1

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