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: 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: 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: rs1800871
rs1800871
IL10 ; IL19
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.830 0.800 5 2010 2017
dbSNP: rs1800896
rs1800896
IL10 ; IL19
0.507 0.800 1 206773552 intron variant T/C snv 0.41
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.050 1.000 5 2010 2019
dbSNP: rs1800896
rs1800896
IL10 ; IL19
0.507 0.800 1 206773552 intron variant T/C snv 0.41
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke 		0.050 0.800 5 2010 2020
dbSNP: rs1518111
rs1518111
IL10 ; IL19
0.790 0.360 1 206771300 intron variant T/C snv 0.71
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.830 1.000 4 2010 2015
dbSNP: rs1800871
rs1800871
IL10 ; IL19
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.040 0.750 4 2012 2018
dbSNP: rs1800871
rs1800871
IL10 ; IL19
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		0.040 0.750 4 2012 2018
dbSNP: rs1800871
rs1800871
IL10 ; IL19
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		0.040 1.000 4 2011 2019
dbSNP: rs1800871
rs1800871
IL10 ; IL19
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach 		0.040 1.000 4 2011 2019
dbSNP: rs1800872
rs1800872
IL10 ; IL19
0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.040 1.000 4 2012 2014
dbSNP: rs1800896
rs1800896
IL10 ; IL19
0.507 0.800 1 206773552 intron variant T/C snv 0.41
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.040 0.750 4 2009 2014
dbSNP: rs1800896
rs1800896
IL10 ; IL19
0.507 0.800 1 206773552 intron variant T/C snv 0.41
CUI: C0011884
Disease: Diabetic Retinopathy
Diabetic Retinopathy 		0.040 1.000 4 2017 2019
dbSNP: rs1800896
rs1800896
IL10 ; IL19
0.507 0.800 1 206773552 intron variant T/C snv 0.41
CUI: C0041296
Disease: Tuberculosis
Tuberculosis 		0.040 0.750 4 2015 2020