Variants studied for Maturity-onset diabetes of the young type 4

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
1	5	10	4	4	23

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
PDX1	1	5	10	4	4	23

Submitter and significance breakdown #

Total submitters: 13

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Submitter	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	total
Women's Health and Genetics/Laboratory Corporation of America, LabCorp	0	3	2	2	1	8
Broad Center for Mendelian Genomics, Broad Institute of MIT and Harvard	1	0	1	0	2	4
Mendelics	0	0	1	1	2	4
Department Of Endocrinology, Sanjay Gandhi Postgraduate Institute Of Medical Sciences	0	0	1	1	0	2
OMIM	1	0	1	0	0	2
Clinical Genomics Laboratory, Washington University in St. Louis	1	0	0	0	0	1
Department of Laboratory Medicine, Seoul National University Bundang Hospital	0	1	0	0	0	1
Genomics Laboratory, Virgen de la Arrixaca University Clinical Hospital	0	0	1	0	0	1
Institute for Human Genetics and Genomic Medicine, Uniklinik RWTH Aachen	0	0	1	0	0	1
Institute of Medical Genetics and Applied Genomics, University Hospital Tübingen	0	0	1	0	0	1
Molecular Genetics, Royal Melbourne Hospital	0	0	1	0	0	1
Neuberg Centre For Genomic Medicine, NCGM	0	0	1	0	0	1
Seattle Children's Hospital Molecular Genetics Laboratory, Seattle Children's Hospital	0	1	0	0	0	1

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