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: 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: 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: rs1518111
rs1518111
IL10 ; IL19
0.790 0.360 1 206771300 intron variant T/C snv 0.71
CUI: C0018681
Disease: Headache
Headache 		0.010 1.000 1 2018 2018
dbSNP: rs1518111
rs1518111
IL10 ; IL19
0.790 0.360 1 206771300 intron variant T/C snv 0.71
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		0.010 1.000 1 2018 2018
dbSNP: rs1518111
rs1518111
IL10 ; IL19
0.790 0.360 1 206771300 intron variant T/C snv 0.71
CUI: C0023290
Disease: Leishmaniasis, Visceral
Leishmaniasis, Visceral 		0.010 1.000 1 2015 2015
dbSNP: rs1518111
rs1518111
IL10 ; IL19
0.790 0.360 1 206771300 intron variant T/C snv 0.71
CUI: C0041327
Disease: Tuberculosis, Pulmonary
Tuberculosis, Pulmonary 		0.010 1.000 1 2018 2018
dbSNP: rs1518111
rs1518111
IL10 ; IL19
0.790 0.360 1 206771300 intron variant T/C snv 0.71
CUI: C0409974
Disease: Lupus Erythematosus
Lupus Erythematosus 		0.010 1.000 1 2018 2018
dbSNP: rs1518111
rs1518111
IL10 ; IL19
0.790 0.360 1 206771300 intron variant T/C snv 0.71
CUI: C0024138
Disease: Lupus Erythematosus, Discoid
Lupus Erythematosus, Discoid 		0.010 1.000 1 2018 2018
dbSNP: rs1518111
rs1518111
IL10 ; IL19
0.790 0.360 1 206771300 intron variant T/C snv 0.71
CUI: C0024131
Disease: Lupus Vulgaris
Lupus Vulgaris 		0.010 1.000 1 2018 2018
dbSNP: rs1518111
rs1518111
IL10 ; IL19
0.790 0.360 1 206771300 intron variant T/C snv 0.71
CUI: C0026918
Disease: Mycobacterium Infections
Mycobacterium Infections 		0.010 1.000 1 2017 2017
dbSNP: rs1554286
rs1554286
IL10 ; IL19
0.790 0.320 1 206770888 5 prime UTR variant A/G;T snv 0.72
CUI: C0014541
Disease: Epiglottitis
Epiglottitis 		0.010 1.000 1 2010 2010
dbSNP: rs1554286
rs1554286
IL10 ; IL19
0.790 0.320 1 206770888 5 prime UTR variant A/G;T snv 0.72
CUI: C0023343
Disease: Leprosy
Leprosy 		0.010 1.000 1 2011 2011
dbSNP: rs1554286
rs1554286
IL10 ; IL19
0.790 0.320 1 206770888 5 prime UTR variant A/G;T snv 0.72
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke 		0.010 1.000 1 2013 2013
dbSNP: rs1554286
rs1554286
IL10 ; IL19
0.790 0.320 1 206770888 5 prime UTR variant A/G;T snv 0.72
CUI: C0041327
Disease: Tuberculosis, Pulmonary
Tuberculosis, Pulmonary 		0.010 1.000 1 2018 2018
dbSNP: rs1554286
rs1554286
IL10 ; IL19
0.790 0.320 1 206770888 5 prime UTR variant A/G;T snv 0.72
CUI: C0023290
Disease: Leishmaniasis, Visceral
Leishmaniasis, Visceral 		0.010 1.000 1 2015 2015
dbSNP: rs1554286
rs1554286
IL10 ; IL19
0.790 0.320 1 206770888 5 prime UTR variant A/G;T snv 0.72
CUI: C0033860
Disease: Psoriasis
Psoriasis 		0.010 1.000 1 2017 2017
dbSNP: rs1800871
rs1800871
IL10 ; IL19
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69
CUI: C0272285
Disease: Heparin-induced thrombocytopenia
Heparin-induced thrombocytopenia 		0.010 1.000 1 2012 2012
dbSNP: rs1800871
rs1800871
IL10 ; IL19
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69
CUI: C0271055
Disease: Rhegmatogenous retinal detachment
Rhegmatogenous retinal detachment 		0.010 1.000 1 2019 2019
dbSNP: rs1800871
rs1800871
IL10 ; IL19
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69
CUI: C0243026
Disease: Sepsis
Sepsis 		0.010 1.000 1 2016 2016
dbSNP: rs1800871
rs1800871
IL10 ; IL19
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69
CUI: C0151281
Disease: Genital ulcers
Genital ulcers 		0.010 1.000 1 2015 2015
dbSNP: rs1800871
rs1800871
IL10 ; IL19
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate 		0.010 < 0.001 1 2011 2011