IRF5, interferon regulatory factor 5, 3663

N. diseases: 226; N. variants: 15
Disease: Sjogren's Syndrome ×
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs3757387
rs3757387 		0.851 0.280 7 128936032 upstream gene variant T/C snv 0.38
CUI: C1527336
Disease: Sjogren's Syndrome
Sjogren's Syndrome 		Eye Diseases; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases; Stomatognathic Diseases 0.700 1.000 1 2013 2013
dbSNP: rs3823536
rs3823536 		0.925 0.280 7 128939612 intron variant G/A snv 0.40
CUI: C1527336
Disease: Sjogren's Syndrome
Sjogren's Syndrome 		Eye Diseases; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases; Stomatognathic Diseases 0.700 1.000 1 2017 2017