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: rs145922845
rs145922845
IL10 ; IL19
1.000 0.040 1 206772393 missense variant C/T snv 1.9E-03 1.8E-03
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.030 0.667 3 2000 2005
dbSNP: rs1373589952
rs1373589952
IL10 ; IL19
1.000 0.120 1 206772296 missense variant G/A snv 7.0E-06
CUI: C2931822
Disease: Nasopharyngeal carcinoma
Nasopharyngeal carcinoma 		0.010 1.000 1 2012 2012
dbSNP: rs1800893
rs1800893
IL10 ; IL19
1.000 0.120 1 206773822 intron variant C/T snv 0.41
CUI: C0024305
Disease: Lymphoma, Non-Hodgkin
Lymphoma, Non-Hodgkin 		0.010 1.000 1 2017 2017
dbSNP: rs3024495
rs3024495
IL10 ; IL19
1.000 0.080 1 206769068 intron variant C/A;T snv
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		0.010 1.000 1 2013 2013
dbSNP: rs3024491
rs3024491
IL10 ; IL19
0.925 0.040 1 206771701 intron variant C/A;T snv
CUI: C0374997
Disease: Helicobacter pylori (H. pylori) infection in conditions classified elsewhere and of unspecified site
Helicobacter pylori (H. pylori) infection in conditions classified elsewhere and of unspecified site 		0.010 1.000 1 2014 2014
dbSNP: rs3024491
rs3024491
IL10 ; IL19
0.925 0.040 1 206771701 intron variant C/A;T snv
CUI: C0850666
Disease: Infection caused by Helicobacter pylori
Infection caused by Helicobacter pylori 		0.010 1.000 1 2014 2014
dbSNP: rs1878672
rs1878672
IL10 ; IL19
0.882 0.080 1 206770368 intron variant G/A;C;T snv
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis 		0.010 1.000 1 2015 2015
dbSNP: rs1878672
rs1878672
IL10 ; IL19
0.882 0.080 1 206770368 intron variant G/A;C;T snv
CUI: C0850666
Disease: Infection caused by Helicobacter pylori
Infection caused by Helicobacter pylori 		0.010 1.000 1 2014 2014
dbSNP: rs1878672
rs1878672
IL10 ; IL19
0.882 0.080 1 206770368 intron variant G/A;C;T snv
CUI: C0374997
Disease: Helicobacter pylori (H. pylori) infection in conditions classified elsewhere and of unspecified site
Helicobacter pylori (H. pylori) infection in conditions classified elsewhere and of unspecified site 		0.010 1.000 1 2014 2014
dbSNP: rs3790622
rs3790622
IL10 ; IL19
0.882 0.320 1 206771818 intron variant G/A snv 1.5E-03
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.010 1.000 1 2014 2014
dbSNP: rs3790622
rs3790622
IL10 ; IL19
0.882 0.320 1 206771818 intron variant G/A snv 1.5E-03
CUI: C0041327
Disease: Tuberculosis, Pulmonary
Tuberculosis, Pulmonary 		0.010 1.000 1 2018 2018
dbSNP: rs3790622
rs3790622
IL10 ; IL19
0.882 0.320 1 206771818 intron variant G/A snv 1.5E-03
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
Non-Small Cell Lung Carcinoma 		0.010 1.000 1 2019 2019
dbSNP: rs1518110
rs1518110
IL10 ; IL19
0.851 0.160 1 206771516 intron variant A/C;T snv
CUI: C0024138
Disease: Lupus Erythematosus, Discoid
Lupus Erythematosus, Discoid 		0.010 1.000 1 2018 2018
dbSNP: rs1518110
rs1518110
IL10 ; IL19
0.851 0.160 1 206771516 intron variant A/C;T snv
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		0.010 1.000 1 2018 2018
dbSNP: rs1518110
rs1518110
IL10 ; IL19
0.851 0.160 1 206771516 intron variant A/C;T snv
CUI: C0409974
Disease: Lupus Erythematosus
Lupus Erythematosus 		0.010 1.000 1 2018 2018
dbSNP: rs1518110
rs1518110
IL10 ; IL19
0.851 0.160 1 206771516 intron variant A/C;T snv
CUI: C0024131
Disease: Lupus Vulgaris
Lupus Vulgaris 		0.010 1.000 1 2018 2018
dbSNP: rs1518110
rs1518110
IL10 ; IL19
0.851 0.160 1 206771516 intron variant A/C;T snv
CUI: C0018681
Disease: Headache
Headache 		0.010 1.000 1 2018 2018
dbSNP: rs2222202
rs2222202
IL10 ; IL19
0.827 0.160 1 206772036 intron variant G/A snv 0.39
CUI: C0042164
Disease: Uveitis
Uveitis 		0.010 1.000 1 2010 2010
dbSNP: rs2222202
rs2222202
IL10 ; IL19
0.827 0.160 1 206772036 intron variant G/A snv 0.39
CUI: C1843273
Disease: Tubulointerstitial nephritis and uveitis
Tubulointerstitial nephritis and uveitis 		0.010 1.000 1 2019 2019
dbSNP: rs2222202
rs2222202
IL10 ; IL19
0.827 0.160 1 206772036 intron variant G/A snv 0.39
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.010 1.000 1 2009 2009
dbSNP: rs2222202
rs2222202
IL10 ; IL19
0.827 0.160 1 206772036 intron variant G/A snv 0.39
CUI: C0027707
Disease: Nephritis, Interstitial
Nephritis, Interstitial 		0.010 1.000 1 2019 2019
dbSNP: rs2222202
rs2222202
IL10 ; IL19
0.827 0.160 1 206772036 intron variant G/A snv 0.39
CUI: C0041349
Disease: Nephritis, Tubulointerstitial
Nephritis, Tubulointerstitial 		0.010 1.000 1 2019 2019
dbSNP: rs3021094
rs3021094
IL10 ; IL19
0.827 0.360 1 206771607 intron variant T/G snv 8.0E-02
CUI: C0014061
Disease: Tick-Borne Encephalitis
Tick-Borne Encephalitis 		0.010 1.000 1 2016 2016
dbSNP: rs3021094
rs3021094
IL10 ; IL19
0.827 0.360 1 206771607 intron variant T/G snv 8.0E-02
CUI: C0027651
Disease: Neoplasms
Neoplasms 		0.010 1.000 1 2013 2013
dbSNP: rs3021094
rs3021094
IL10 ; IL19
0.827 0.360 1 206771607 intron variant T/G snv 8.0E-02
CUI: C1269955
Disease: Tumor Cell Invasion
Tumor Cell Invasion 		0.010 1.000 1 2013 2013