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: rs3024498
rs3024498
IL10
0.790 0.360 1 206768184 3 prime UTR variant T/C snv 0.20
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.010 1.000 1 2015 2015
dbSNP: rs3024498
rs3024498
IL10
0.790 0.360 1 206768184 3 prime UTR variant T/C snv 0.20
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		0.010 1.000 1 2018 2018
dbSNP: rs3024498
rs3024498
IL10
0.790 0.360 1 206768184 3 prime UTR variant T/C snv 0.20
CUI: C0014061
Disease: Tick-Borne Encephalitis
Tick-Borne Encephalitis 		0.010 1.000 1 2016 2016
dbSNP: rs3024498
rs3024498
IL10
0.790 0.360 1 206768184 3 prime UTR variant T/C snv 0.20
CUI: C0018889
Disease: Helminthiasis
Helminthiasis 		0.010 1.000 1 2013 2013
dbSNP: rs3024498
rs3024498
IL10
0.790 0.360 1 206768184 3 prime UTR variant T/C snv 0.20
CUI: C0023290
Disease: Leishmaniasis, Visceral
Leishmaniasis, Visceral 		0.010 1.000 1 2015 2015
dbSNP: rs3024498
rs3024498
IL10
0.790 0.360 1 206768184 3 prime UTR variant T/C snv 0.20
CUI: C0041296
Disease: Tuberculosis
Tuberculosis 		0.010 1.000 1 2011 2011
dbSNP: rs3024498
rs3024498
IL10
0.790 0.360 1 206768184 3 prime UTR variant T/C snv 0.20
CUI: C0003864
Disease: Arthritis
Arthritis 		0.010 1.000 1 2018 2018
dbSNP: rs3024496
rs3024496
IL10
0.827 0.200 1 206768519 3 prime UTR variant A/G snv 0.43
CUI: C0037284
Disease: Skin lesion
Skin lesion 		0.010 1.000 1 2015 2015
dbSNP: rs3024496
rs3024496
IL10
0.827 0.200 1 206768519 3 prime UTR variant A/G snv 0.43
CUI: C0007114
Disease: Malignant neoplasm of skin
Malignant neoplasm of skin 		0.010 1.000 1 2015 2015
dbSNP: rs3024496
rs3024496
IL10
0.827 0.200 1 206768519 3 prime UTR variant A/G snv 0.43
CUI: C0850666
Disease: Infection caused by Helicobacter pylori
Infection caused by Helicobacter pylori 		0.010 1.000 1 2014 2014
dbSNP: rs3024496
rs3024496
IL10
0.827 0.200 1 206768519 3 prime UTR variant A/G snv 0.43
CUI: C0014175
Disease: Endometriosis
Endometriosis 		0.010 1.000 1 2017 2017
dbSNP: rs3024496
rs3024496
IL10
0.827 0.200 1 206768519 3 prime UTR variant A/G snv 0.43
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate 		0.010 1.000 1 2009 2009
dbSNP: rs3024496
rs3024496
IL10
0.827 0.200 1 206768519 3 prime UTR variant A/G snv 0.43
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		0.010 1.000 1 2009 2009
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: 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: rs3024493
rs3024493
IL10 ; IL19
0.776 0.280 1 206770623 intron variant C/A;T snv 0.11
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		0.720 1.000 4 2013 2019
dbSNP: rs3024493
rs3024493
IL10 ; IL19
0.776 0.280 1 206770623 intron variant C/A;T snv 0.11
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		0.800 1.000 3 2009 2016
dbSNP: rs3024493
rs3024493
IL10 ; IL19
0.776 0.280 1 206770623 intron variant C/A;T snv 0.11
CUI: C0033860
Disease: Psoriasis
Psoriasis 		0.700 1.000 1 2016 2016
dbSNP: rs3024493
rs3024493
IL10 ; IL19
0.776 0.280 1 206770623 intron variant C/A;T snv 0.11
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.700 1.000 1 2016 2016
dbSNP: rs3024493
rs3024493
IL10 ; IL19
0.776 0.280 1 206770623 intron variant C/A;T snv 0.11
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
Diabetes Mellitus, Insulin-Dependent 		0.700 1.000 1 2011 2011
dbSNP: rs3024493
rs3024493
IL10 ; IL19
0.776 0.280 1 206770623 intron variant C/A;T snv 0.11
CUI: C0008313
Disease: Cholangitis, Sclerosing
Cholangitis, Sclerosing 		0.700 1.000 1 2016 2016
dbSNP: rs3024493
rs3024493
IL10 ; IL19
0.776 0.280 1 206770623 intron variant C/A;T snv 0.11
CUI: C0025202
Disease: melanoma
melanoma 		0.010 1.000 1 2015 2015
dbSNP: rs3024493
rs3024493
IL10 ; IL19
0.776 0.280 1 206770623 intron variant C/A;T snv 0.11
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis 		0.700 1.000 1 2016 2016