Variants studied for type 1 diabetes mellitus 20

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
18	11	119	16	1	165

Gene and significance breakdown #

Total genes and gene combinations: 3

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Gene or gene combination	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	total
HNF1A	18	11	105	16	1	151
C12orf43, HNF1A	0	0	13	0	0	13
KCNJ11	0	0	1	0	0	1

Submitter and significance breakdown #

Total submitters: 6

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Submitter	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	total
Fulgent Genetics, Fulgent Genetics	12	11	106	16	1	146
Baylor Genetics	0	0	7	0	0	7
New York Genome Center	0	0	7	0	0	7
OMIM	4	0	0	0	0	4
Genetics and Molecular Pathology, SA Pathology	2	0	0	0	0	2
Institute of Human Genetics, University of Leipzig Medical Center	0	0	1	0	0	1

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