rs3021094, IL10;IL19

N. diseases: 8
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Behcet Syndrome
CUI: C0004943
Disease: Behcet Syndrome
243 0.827 0.360 1 206771607 intron variant T/G snv 8.0E-02 0.010 1.000 1 2014 2014
Gestational Diabetes
CUI: C0085207
Disease: Gestational Diabetes
224 0.827 0.360 1 206771607 intron variant T/G snv 8.0E-02 0.010 1.000 1 2019 2019
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
704 0.827 0.360 1 206771607 intron variant T/G snv 8.0E-02 0.010 1.000 1 2013 2013
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.827 0.360 1 206771607 intron variant T/G snv 8.0E-02 0.010 1.000 1 2013 2013
Non-Small Cell Lung Carcinoma
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
712 0.827 0.360 1 206771607 intron variant T/G snv 8.0E-02 0.010 1.000 1 2019 2019
Tick-Borne Encephalitis
CUI: C0014061
Disease: Tick-Borne Encephalitis
9 0.827 0.360 1 206771607 intron variant T/G snv 8.0E-02 0.010 1.000 1 2016 2016
Tuberculosis, Pulmonary
CUI: C0041327
Disease: Tuberculosis, Pulmonary
171 0.827 0.360 1 206771607 intron variant T/G snv 8.0E-02 0.010 1.000 1 2018 2018
Tumor Cell Invasion
CUI: C1269955
Disease: Tumor Cell Invasion
169 0.827 0.360 1 206771607 intron variant T/G snv 8.0E-02 0.010 1.000 1 2013 2013