Source: GWASCAT

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: rs1107345
rs1107345
0.925 0.160 10 6045332 intron variant G/T snv 0.18
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.700 1.000 1 2019 2019
dbSNP: rs1107345
rs1107345
0.925 0.160 10 6045332 intron variant G/T snv 0.18
CUI: C1367654
Disease: Marginal Zone B-Cell Lymphoma
Marginal Zone B-Cell Lymphoma
0.700 1.000 1 2019 2019
dbSNP: rs12253981
rs12253981
1.000 0.080 10 6050383 intron variant T/G snv 0.29
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.700 1.000 1 2017 2017
dbSNP: rs12722486
rs12722486
1.000 10 6061799 intron variant C/A;T snv
HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO
0.700 1.000 1 2014 2014
dbSNP: rs12722486
rs12722486
1.000 10 6061799 intron variant C/A;T snv
CUI: C0442874
Disease: Neuropathy
Neuropathy
0.700 1.000 1 2014 2014
dbSNP: rs12722486
rs12722486
1.000 10 6061799 intron variant C/A;T snv
ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO
0.700 1.000 1 2014 2014
dbSNP: rs12722486
rs12722486
1.000 10 6061799 intron variant C/A;T snv
CUI: C1836233
Disease: AIDS, PROGRESSION TO
AIDS, PROGRESSION TO
0.700 1.000 1 2014 2014
dbSNP: rs12722486
rs12722486
1.000 10 6061799 intron variant C/A;T snv
CUI: C1836231
Disease: HIV-1, RESISTANCE TO
HIV-1, RESISTANCE TO
0.700 1.000 1 2014 2014
dbSNP: rs12722489
rs12722489
0.882 0.160 10 6060049 intron variant C/T snv 0.11
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.850 1.000 2 2007 2018
dbSNP: rs12722489
rs12722489
0.882 0.160 10 6060049 intron variant C/T snv 0.11
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.800 1.000 1 2010 2010
dbSNP: rs12722495
rs12722495
0.851 0.200 10 6055320 intron variant T/C snv 7.0E-02
Diabetes Mellitus, Insulin-Dependent
0.710 1.000 1 2011 2019
dbSNP: rs12722502
rs12722502
0.882 0.080 10 6051176 intron variant C/T snv 7.8E-03
CUI: C0004096
Disease: Asthma
Asthma
0.700 1.000 2 2019 2019
dbSNP: rs12722502
rs12722502
0.882 0.080 10 6051176 intron variant C/T snv 7.8E-03
CUI: C0741260
Disease: Adult onset asthma
Adult onset asthma
0.700 1.000 1 2019 2019
dbSNP: rs12722502
rs12722502
0.882 0.080 10 6051176 intron variant C/T snv 7.8E-03
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2019 2019
dbSNP: rs12722502
rs12722502
0.882 0.080 10 6051176 intron variant C/T snv 7.8E-03
CUI: C0264408
Disease: Childhood asthma
Childhood asthma
0.700 1.000 1 2019 2019
dbSNP: rs12722515
rs12722515
1.000 0.040 10 6039267 intron variant C/A snv 0.13
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases
0.800 1.000 2 2012 2015
dbSNP: rs12722515
rs12722515
1.000 0.040 10 6039267 intron variant C/A snv 0.13
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.700 1.000 1 2015 2015
dbSNP: rs12722547
rs12722547
10 6030130 intron variant G/C snv 7.8E-03
CUI: C0035242
Disease: Respiratory Tract Diseases
Respiratory Tract Diseases
0.700 1.000 1 2019 2019
dbSNP: rs12722561
rs12722561
1.000 0.080 10 6027930 intron variant C/A;T snv
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.700 1.000 1 2016 2016
dbSNP: rs2104286
rs2104286
0.662 0.440 10 6057082 intron variant T/C snv 0.18
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.900 1.000 2 2007 2019
dbSNP: rs2104286
rs2104286
0.662 0.440 10 6057082 intron variant T/C snv 0.18
CUI: C0008313
Disease: Cholangitis, Sclerosing
Cholangitis, Sclerosing
0.700 1.000 1 2016 2016
dbSNP: rs2104286
rs2104286
0.662 0.440 10 6057082 intron variant T/C snv 0.18
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis
0.700 1.000 1 2016 2016
dbSNP: rs2104286
rs2104286
0.662 0.440 10 6057082 intron variant T/C snv 0.18
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.830 1.000 1 2012 2015
dbSNP: rs2104286
rs2104286
0.662 0.440 10 6057082 intron variant T/C snv 0.18
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.700 1.000 1 2016 2016
dbSNP: rs2104286
rs2104286
0.662 0.440 10 6057082 intron variant T/C snv 0.18
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis
0.700 1.000 1 2016 2016