Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1861493
rs1861493
IFNG ; IFNG-AS1
0.851 0.280 12 68157416 intron variant G/A snv 0.76
CUI: C0004096
Disease: Asthma
Asthma 		0.010 1.000 1 2008 2008
dbSNP: rs1861493
rs1861493
IFNG ; IFNG-AS1
0.851 0.280 12 68157416 intron variant G/A snv 0.76
CUI: C1842937
Disease: AURAL ATRESIA, CONGENITAL
AURAL ATRESIA, CONGENITAL 		0.010 1.000 1 2016 2016
dbSNP: rs1861493
rs1861493
IFNG ; IFNG-AS1
0.851 0.280 12 68157416 intron variant G/A snv 0.76
CUI: C0041327
Disease: Tuberculosis, Pulmonary
Tuberculosis, Pulmonary 		0.010 1.000 1 2012 2012
dbSNP: rs1861493
rs1861493
IFNG ; IFNG-AS1
0.851 0.280 12 68157416 intron variant G/A snv 0.76
CUI: C0026691
Disease: Mucocutaneous Lymph Node Syndrome
Mucocutaneous Lymph Node Syndrome 		0.010 1.000 1 2016 2016
dbSNP: rs1861494
rs1861494
IFNG ; IFNG-AS1
0.716 0.400 12 68157629 intron variant C/T snv 0.75
CUI: C0041296
Disease: Tuberculosis
Tuberculosis 		0.030 1.000 3 2015 2019
dbSNP: rs1861494
rs1861494
IFNG ; IFNG-AS1
0.716 0.400 12 68157629 intron variant C/T snv 0.75
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 		0.010 1.000 1 2014 2014
dbSNP: rs1861494
rs1861494
IFNG ; IFNG-AS1
0.716 0.400 12 68157629 intron variant C/T snv 0.75
CUI: C0022104
Disease: Irritable Bowel Syndrome
Irritable Bowel Syndrome 		0.010 1.000 1 2014 2014
dbSNP: rs1861494
rs1861494
IFNG ; IFNG-AS1
0.716 0.400 12 68157629 intron variant C/T snv 0.75
CUI: C0155877
Disease: Allergic asthma
Allergic asthma 		0.010 1.000 1 2008 2008
dbSNP: rs1861494
rs1861494
IFNG ; IFNG-AS1
0.716 0.400 12 68157629 intron variant C/T snv 0.75
CUI: C0041327
Disease: Tuberculosis, Pulmonary
Tuberculosis, Pulmonary 		0.010 1.000 1 2012 2012
dbSNP: rs1861494
rs1861494
IFNG ; IFNG-AS1
0.716 0.400 12 68157629 intron variant C/T snv 0.75
CUI: C0018553
Disease: Hamartoma Syndrome, Multiple
Hamartoma Syndrome, Multiple 		0.010 1.000 1 2014 2014
dbSNP: rs1861494
rs1861494
IFNG ; IFNG-AS1
0.716 0.400 12 68157629 intron variant C/T snv 0.75
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		0.010 1.000 1 2014 2014
dbSNP: rs1861494
rs1861494
IFNG ; IFNG-AS1
0.716 0.400 12 68157629 intron variant C/T snv 0.75
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.010 1.000 1 2014 2014
dbSNP: rs1861494
rs1861494
IFNG ; IFNG-AS1
0.716 0.400 12 68157629 intron variant C/T snv 0.75
CUI: C0042900
Disease: Vitiligo
Vitiligo 		0.010 1.000 1 2017 2017
dbSNP: rs1861494
rs1861494
IFNG ; IFNG-AS1
0.716 0.400 12 68157629 intron variant C/T snv 0.75
CUI: C0038443
Disease: Stress, Psychological
Stress, Psychological 		0.010 1.000 1 2015 2015
dbSNP: rs1861494
rs1861494
IFNG ; IFNG-AS1
0.716 0.400 12 68157629 intron variant C/T snv 0.75
CUI: C1827849
Disease: IgE-mediated allergic asthma
IgE-mediated allergic asthma 		0.010 1.000 1 2008 2008
dbSNP: rs1861494
rs1861494
IFNG ; IFNG-AS1
0.716 0.400 12 68157629 intron variant C/T snv 0.75
CUI: C0004096
Disease: Asthma
Asthma 		0.010 1.000 1 2008 2008
dbSNP: rs1861494
rs1861494
IFNG ; IFNG-AS1
0.716 0.400 12 68157629 intron variant C/T snv 0.75
CUI: C0017661
Disease: IGA Glomerulonephritis
IGA Glomerulonephritis 		0.010 1.000 1 2017 2017
dbSNP: rs1861494
rs1861494
IFNG ; IFNG-AS1
0.716 0.400 12 68157629 intron variant C/T snv 0.75
CUI: C1609538
Disease: Latent Tuberculosis
Latent Tuberculosis 		0.010 1.000 1 2019 2019
dbSNP: rs1861494
rs1861494
IFNG ; IFNG-AS1
0.716 0.400 12 68157629 intron variant C/T snv 0.75
CUI: C1847835
Disease: VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 1 (finding)
VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 1 (finding) 		0.010 1.000 1 2017 2017
dbSNP: rs2069718
rs2069718
IFNG ; IFNG-AS1
0.742 0.320 12 68156382 intron variant A/G;T snv 0.50
CUI: C0041330
Disease: Tuberculosis, Spinal
Tuberculosis, Spinal 		0.010 1.000 1 2017 2017
dbSNP: rs2069718
rs2069718
IFNG ; IFNG-AS1
0.742 0.320 12 68156382 intron variant A/G;T snv 0.50
CUI: C0019270
Disease: Hernia
Hernia 		0.010 1.000 1 2017 2017
dbSNP: rs2069718
rs2069718
IFNG ; IFNG-AS1
0.742 0.320 12 68156382 intron variant A/G;T snv 0.50
CUI: C0038644
Disease: Sudden infant death syndrome
Sudden infant death syndrome 		0.010 1.000 1 2019 2019
dbSNP: rs2069718
rs2069718
IFNG ; IFNG-AS1
0.742 0.320 12 68156382 intron variant A/G;T snv 0.50
CUI: C0030193
Disease: Pain
Pain 		0.010 1.000 1 2017 2017
dbSNP: rs2069718
rs2069718
IFNG ; IFNG-AS1
0.742 0.320 12 68156382 intron variant A/G;T snv 0.50
CUI: C0007766
Disease: Intracranial Aneurysm
Intracranial Aneurysm 		0.010 1.000 1 2015 2015
dbSNP: rs2069718
rs2069718
IFNG ; IFNG-AS1
0.742 0.320 12 68156382 intron variant A/G;T snv 0.50
CUI: C0041327
Disease: Tuberculosis, Pulmonary
Tuberculosis, Pulmonary 		0.010 1.000 1 2017 2017