NFKBIE, NFKB inhibitor epsilon, 4794

N. diseases: 26; N. variants: 6
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: rs2233434
rs2233434
1.000 0.120 6 44265183 missense variant A/G snv 4.9E-02 5.1E-02
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases 0.810 1.000 3 2012 2016
dbSNP: rs2233424
rs2233424
1.000 0.120 6 44266184 upstream gene variant C/G;T snv
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases 0.800 1.000 2 2014 2019
dbSNP: rs730775
rs730775
1.000 0.080 6 44264337 intron variant A/G snv 0.36
CUI: C0200637
Disease: Monocyte count procedure
Monocyte count procedure
0.700 1.000 1 2016 2016
dbSNP: rs730775
rs730775
1.000 0.080 6 44264337 intron variant A/G snv 0.36
CUI: C0750880
Disease: Monocyte count result
Monocyte count result
0.700 1.000 1 2016 2016
dbSNP: rs2233437
rs2233437
1.000 0.080 6 44260425 intron variant G/A snv 0.43 0.35
CUI: C0019196
Disease: Hepatitis C
Hepatitis C
Digestive System Diseases; Infections 0.010 1.000 1 2014 2014
dbSNP: rs2282151
rs2282151
0.925 0.080 6 44258458 3 prime UTR variant T/C snv 0.17
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
Digestive System Diseases; Neoplasms 0.010 1.000 1 2016 2016
dbSNP: rs2282151
rs2282151
0.925 0.080 6 44258458 3 prime UTR variant T/C snv 0.17
Malignant neoplasm of colon and/or rectum
0.010 1.000 1 2016 2016
dbSNP: rs28362857
rs28362857
1.000 0.080 6 44265479 missense variant G/A;C snv 8.3E-06; 3.1E-02
CUI: C0019196
Disease: Hepatitis C
Hepatitis C
Digestive System Diseases; Infections 0.010 1.000 1 2014 2014
dbSNP: rs730775
rs730775
1.000 0.080 6 44264337 intron variant A/G snv 0.36
CUI: C0019196
Disease: Hepatitis C
Hepatitis C
Digestive System Diseases; Infections 0.010 1.000 1 2014 2014