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
2	6	21	8	4	40

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	2	6	21	8	4	40

Submitter and significance breakdown #

Total submitters: 15

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Submitter	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	total
Fulgent Genetics, Fulgent Genetics	1	0	8	3	0	12
Women's Health and Genetics/Laboratory Corporation of America, LabCorp	0	3	2	3	1	9
Mendelics	0	0	1	1	2	4
Broad Center for Mendelian Genomics, Broad Institute of MIT and Harvard	1	0	1	0	2	4
New York Genome Center	0	0	4	0	0	4
Genetic Services Laboratory, University of Chicago	2	1	0	0	0	3
OMIM	1	0	1	0	0	2
Department Of Endocrinology, Sanjay Gandhi Postgraduate Institute Of Medical Sciences	0	0	1	1	0	2
Institute for Human Genetics and Genomic Medicine, Uniklinik RWTH Aachen	0	0	1	0	0	1
Juno Genomics, Hangzhou Juno Genomics, Inc	0	0	1	0	0	1
Institute of Medical Genetics and Applied Genomics, University Hospital Tübingen	0	0	1	0	0	1
Seattle Children's Hospital Molecular Genetics Laboratory, Seattle Children's Hospital	0	1	0	0	0	1
Neuberg Centre For Genomic Medicine, NCGM	0	0	1	0	0	1
Molecular Genetics, Royal Melbourne Hospital	0	0	1	0	0	1
Department of Laboratory Medicine, Seoul National University Bundang Hospital	0	1	0	0	0	1

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