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: rs1518111
rs1518111
0.878 0.250 1 206771300 intron variant T/C snp 0.71
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.830 1.000 4 2010 2016
dbSNP: rs1800871
rs1800871
0.602 0.643 1 206773289 intergenic variant A/G snp 0.69
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.820 1.000 4 2010 2016
dbSNP: rs3024493
rs3024493
0.769 0.250 1 206770623 intron variant C/A snp 0.11
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis
0.800 3 2010 2017
dbSNP: rs3024493
rs3024493
0.769 0.250 1 206770623 intron variant C/A snp 0.11
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic
0.710 1.000 2 2014 2016
dbSNP: rs1800872
rs1800872
0.608 0.643 1 206773062 regulatory region variant T/G snp 0.69
HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO
0.700 3 2001 2003
dbSNP: rs3024490
rs3024490
0.846 0.250 1 206771966 intron variant A/C,G,T snp 0.69; 9.6E-05
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.700 1 2013 2013
dbSNP: rs3024493
rs3024493
0.769 0.250 1 206770623 intron variant C/A snp 0.11
CUI: C0033860
Disease: Psoriasis
Psoriasis
0.700 1 2017 2017
dbSNP: rs3024493
rs3024493
0.769 0.250 1 206770623 intron variant C/A snp 0.11
CUI: C0008313
Disease: Cholangitis, Sclerosing
Cholangitis, Sclerosing
0.700 1 2017 2017
dbSNP: rs3024493
rs3024493
0.769 0.250 1 206770623 intron variant C/A snp 0.11
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.700 1 2017 2017
dbSNP: rs3024493
rs3024493
0.769 0.250 1 206770623 intron variant C/A snp 0.11
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis
0.700 1 2017 2017
dbSNP: rs3024493
rs3024493
0.769 0.250 1 206770623 intron variant C/A snp 0.11
Diabetes Mellitus, Insulin-Dependent
0.700 1 2012 2012
dbSNP: rs3024493
rs3024493
0.769 0.250 1 206770623 intron variant C/A snp 0.11
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases
0.700 1 2016 2016
dbSNP: rs1800871
rs1800871
0.602 0.643 1 206773289 intergenic variant A/G snp 0.69
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.030 1.000 3 2011 2013
dbSNP: rs1800871
rs1800871
0.602 0.643 1 206773289 intergenic variant A/G snp 0.69
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
0.030 1.000 3 2011 2013
dbSNP: rs1554286
rs1554286
0.821 0.321 1 206770888 intron variant A/G,T snp 0.72 0.73
CUI: C0023343
Disease: Leprosy
Leprosy
0.020 1.000 2 2011 2016
dbSNP: rs1554286
rs1554286
0.821 0.321 1 206770888 intron variant A/G,T snp 0.72 0.73
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.020 1.000 2 2012 2016
dbSNP: rs1800871
rs1800871
0.602 0.643 1 206773289 intergenic variant A/G snp 0.69
CUI: C0302592
Disease: Cervix carcinoma
Cervix carcinoma
0.020 1.000 2 2015 2016
dbSNP: rs1800871
rs1800871
0.602 0.643 1 206773289 intergenic variant A/G snp 0.69
CUI: C4048328
Disease: cervical cancer
cervical cancer
0.020 1.000 2 2015 2016
dbSNP: rs1800871
rs1800871
0.602 0.643 1 206773289 intergenic variant A/G snp 0.69
CUI: C0007847
Disease: Malignant tumor of cervix
Malignant tumor of cervix
0.020 1.000 2 2015 2016
dbSNP: rs1800871
rs1800871
0.602 0.643 1 206773289 intergenic variant A/G snp 0.69
CUI: C0024305
Disease: Lymphoma, Non-Hodgkin
Lymphoma, Non-Hodgkin
0.020 1.000 2 2011 2015
dbSNP: rs1800871
rs1800871
0.602 0.643 1 206773289 intergenic variant A/G snp 0.69
CUI: C0079744
Disease: Diffuse Large B-Cell Lymphoma
Diffuse Large B-Cell Lymphoma
0.020 1.000 2 2015 2017
dbSNP: rs1800872
rs1800872
0.608 0.643 1 206773062 regulatory region variant T/G snp 0.69
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases
0.020 1.000 2 2014 2018
dbSNP: rs1800872
rs1800872
0.608 0.643 1 206773062 regulatory region variant T/G snp 0.69
CUI: C4048328
Disease: cervical cancer
cervical cancer
0.020 1.000 2 2015 2016
dbSNP: rs1800872
rs1800872
0.608 0.643 1 206773062 regulatory region variant T/G snp 0.69
CUI: C0007847
Disease: Malignant tumor of cervix
Malignant tumor of cervix
0.020 1.000 2 2015 2016
dbSNP: rs1800872
rs1800872
0.608 0.643 1 206773062 regulatory region variant T/G snp 0.69
CUI: C0302592
Disease: Cervix carcinoma
Cervix carcinoma
0.020 1.000 2 2015 2016