Variants studied for Rheumatoid arthritis

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	affects	association	risk factor	total
4	1	3	0	0	1	2	6	17

Gene and significance breakdown #

Total genes and gene combinations: 11

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Gene or gene combination	pathogenic	likely pathogenic	uncertain significance	affects	association	risk factor	total
CIITA	0	1	2	0	0	1	4
AP4B1, PTPN22	0	0	1	0	0	1	2
PADI4	0	0	0	0	2	0	2
TLR1	2	0	0	0	0	0	2
CD244	0	0	0	0	0	1	1
CHRNG	1	0	0	0	0	0	1
IRF5	1	0	0	0	0	0	1
NFKBIL1	0	0	0	0	0	1	1
SLC22A4	0	0	0	0	0	1	1
SOCS1	0	0	0	1	0	0	1
SUPT20H	0	0	0	0	0	1	1

Submitter and significance breakdown #

Total submitters: 8

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Submitter	pathogenic	likely pathogenic	uncertain significance	affects	association	risk factor	total
OMIM	1	0	0	0	0	5	6
Institute of Biochemistry and Biotechnology, Faculty of Life Sciences, University of the Punjab	3	0	0	0	0	0	3
Department of Zoology, University of the Punjab, Lahore	0	0	0	0	2	0	2
Neuberg Supratech Reference Laboratories Pvt Ltd, Neuberg Centre for Genomic Medicine	0	0	2	0	0	0	2
Baylor Genetics	0	0	1	0	0	0	1
Mendelics	0	1	0	0	0	0	1
GenHotel - European Research Laboratory for Rheumatoid Arthritis, University of Paris Saclay	0	0	0	0	0	1	1
Centro Nacional de Biotecnologia, Consejo Superior de Investigaciones Cientificas	0	0	0	1	0	0	1

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