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: rs1554286
rs1554286
0.790 0.320 1 206770888 5 prime UTR variant A/G;T snv 0.72
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.030 1.000 3 2012 2015
dbSNP: rs3024490
rs3024490
0.742 0.520 1 206771966 intron variant A/C;G;T snv
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.710 0.500 2 2013 2017
dbSNP: rs1518110
rs1518110
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
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
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
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
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: rs1554286
rs1554286
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
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
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
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
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
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: rs1878672
rs1878672
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
0.882 0.080 1 206770368 intron variant G/A;C;T snv
Infection caused by Helicobacter pylori
0.010 1.000 1 2014 2014
dbSNP: rs1878672
rs1878672
0.882 0.080 1 206770368 intron variant G/A;C;T snv
Helicobacter pylori (H. pylori) infection in conditions classified elsewhere and of unspecified site
0.010 1.000 1 2014 2014
dbSNP: rs3021097
rs3021097
0.752 0.440 1 206773289 5 prime UTR variant A/G snv
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung
0.010 1.000 1 2014 2014
dbSNP: rs3021097
rs3021097
0.752 0.440 1 206773289 5 prime UTR variant A/G snv
CUI: C2931822
Disease: Nasopharyngeal carcinoma
Nasopharyngeal carcinoma
0.010 1.000 1 2013 2013
dbSNP: rs3021097
rs3021097
0.752 0.440 1 206773289 5 prime UTR variant A/G snv
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung
0.010 1.000 1 2014 2014
dbSNP: rs3021097
rs3021097
0.752 0.440 1 206773289 5 prime UTR variant A/G snv
CUI: C0004096
Disease: Asthma
Asthma
0.010 1.000 1 2016 2016
dbSNP: rs3021097
rs3021097
0.752 0.440 1 206773289 5 prime UTR variant A/G snv
Childhood Acute Lymphoblastic Leukemia
0.010 1.000 1 2017 2017
dbSNP: rs3021097
rs3021097
0.752 0.440 1 206773289 5 prime UTR variant A/G snv
Conventional (Clear Cell) Renal Cell Carcinoma
0.010 1.000 1 2016 2016
dbSNP: rs3021097
rs3021097
0.752 0.440 1 206773289 5 prime UTR variant A/G snv
CUI: C0033860
Disease: Psoriasis
Psoriasis
0.010 < 0.001 1 2019 2019
dbSNP: rs3021097
rs3021097
0.752 0.440 1 206773289 5 prime UTR variant A/G snv
CUI: C1306460
Disease: Primary malignant neoplasm of lung
Primary malignant neoplasm of lung
0.010 1.000 1 2014 2014
dbSNP: rs3021097
rs3021097
0.752 0.440 1 206773289 5 prime UTR variant A/G snv
CUI: C0007134
Disease: Renal Cell Carcinoma
Renal Cell Carcinoma
0.010 1.000 1 2016 2016