rs1861494, IFNG-AS1;IFNG

N. diseases: 15
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Tuberculosis
CUI: C0041296
Disease: Tuberculosis
328 0.716 0.400 12 68157629 intron variant C/T snv 0.75 0.030 1.000 3 2015 2019
Allergic asthma
CUI: C0155877
Disease: Allergic asthma
55 0.716 0.400 12 68157629 intron variant C/T snv 0.75 0.010 1.000 1 2008 2008
Asthma
CUI: C0004096
Disease: Asthma
1536 0.716 0.400 12 68157629 intron variant C/T snv 0.75 0.010 1.000 1 2008 2008
Crohn Disease
CUI: C0010346
Disease: Crohn Disease
1147 0.716 0.400 12 68157629 intron variant C/T snv 0.75 0.010 1.000 1 2014 2014
Hamartoma Syndrome, Multiple
CUI: C0018553
Disease: Hamartoma Syndrome, Multiple
139 0.716 0.400 12 68157629 intron variant C/T snv 0.75 0.010 1.000 1 2014 2014
IGA Glomerulonephritis
CUI: C0017661
Disease: IGA Glomerulonephritis
130 0.716 0.400 12 68157629 intron variant C/T snv 0.75 0.010 1.000 1 2017 2017
IgE-mediated allergic asthma
CUI: C1827849
Disease: IgE-mediated allergic asthma
46 0.716 0.400 12 68157629 intron variant C/T snv 0.75 0.010 1.000 1 2008 2008
Inflammatory Bowel Diseases
CUI: C0021390
Disease: Inflammatory Bowel Diseases
605 0.716 0.400 12 68157629 intron variant C/T snv 0.75 0.010 1.000 1 2014 2014
Irritable Bowel Syndrome
CUI: C0022104
Disease: Irritable Bowel Syndrome
52 0.716 0.400 12 68157629 intron variant C/T snv 0.75 0.010 1.000 1 2014 2014
Latent Tuberculosis
CUI: C1609538
Disease: Latent Tuberculosis
18 0.716 0.400 12 68157629 intron variant C/T snv 0.75 0.010 1.000 1 2019 2019
Stress, Psychological
CUI: C0038443
Disease: Stress, Psychological
24 0.716 0.400 12 68157629 intron variant C/T snv 0.75 0.010 1.000 1 2015 2015
Tuberculosis, Pulmonary
CUI: C0041327
Disease: Tuberculosis, Pulmonary
171 0.716 0.400 12 68157629 intron variant C/T snv 0.75 0.010 1.000 1 2012 2012
Ulcerative Colitis
CUI: C0009324
Disease: Ulcerative Colitis
827 0.716 0.400 12 68157629 intron variant C/T snv 0.75 0.010 1.000 1 2014 2014
Vitiligo
CUI: C0042900
Disease: Vitiligo
249 0.716 0.400 12 68157629 intron variant C/T snv 0.75 0.010 1.000 1 2017 2017
VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 1 (finding)
CUI: C1847835
Disease: VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 1 (finding)
92 0.716 0.400 12 68157629 intron variant C/T snv 0.75 0.010 1.000 1 2017 2017