TNFAIP3, TNF alpha induced protein 3, 7128

N. diseases: 212; N. variants: 29
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: rs5029939
rs5029939
0.701 0.440 6 137874586 intron variant C/G snv 0.13
CUI: C1527336
Disease: Sjogren's Syndrome
Sjogren's Syndrome
Eye Diseases; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases; Stomatognathic Diseases 0.800 1.000 1 2013 2013
dbSNP: rs2230926
rs2230926
0.662 0.440 6 137874929 missense variant T/C;G snv 4.0E-06; 5.4E-02
CUI: C1527336
Disease: Sjogren's Syndrome
Sjogren's Syndrome
Eye Diseases; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases; Stomatognathic Diseases 0.020 1.000 2 2011 2018