Variants studied for Inflammatory bowel disease 25

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	6	118	91	14	229

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
IFNAR2-IL10RB, IL10RB	8	4	106	80	14	201
IFNAR2-IL10RB, IL10RB, LOC130066558	0	2	10	11	0	23
IL10RB	3	0	1	0	0	4
IFNAR2-IL10RB, IL10RB, LOC130066558, LOC130066559, LOC130066560	0	0	1	0	0	1

Submitter and significance breakdown #

Total submitters: 11

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Submitter	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	total
Labcorp Genetics (formerly Invitae), Labcorp	7	3	96	89	9	204
Illumina Laboratory Services, Illumina	0	1	22	3	6	32
Baylor Genetics	0	1	2	0	0	3
OMIM	2	0	0	0	0	2
Clinical Bioinformatic Lab, Royan Institute	1	1	0	0	0	2
Revvity Omics, Revvity	0	0	1	0	0	1
Mendelics	1	0	0	0	0	1
Centre for Mendelian Genomics, University Medical Centre Ljubljana	0	0	1	0	0	1
Center for Genomics, Ann and Robert H. Lurie Children's Hospital of Chicago	0	0	1	0	0	1
Laboratory of Medical Genetics, National & Kapodistrian University of Athens	1	0	0	0	0	1
Laboratorio de Genetica e Diagnostico Molecular, Hospital Israelita Albert Einstein	0	0	1	0	0	1

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