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: rs3118471
rs3118471
0.827 0.120 10 6060794 intron variant A/G snv 0.24
CUI: C0008313
Disease: Cholangitis, Sclerosing
Cholangitis, Sclerosing
0.700 1.000 1 2016 2016
dbSNP: rs3118471
rs3118471
0.827 0.120 10 6060794 intron variant A/G snv 0.24
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis
0.700 1.000 1 2016 2016
dbSNP: rs3118471
rs3118471
0.827 0.120 10 6060794 intron variant A/G snv 0.24
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis
0.700 1.000 1 2016 2016
dbSNP: rs3118471
rs3118471
0.827 0.120 10 6060794 intron variant A/G snv 0.24
CUI: C0033860
Disease: Psoriasis
Psoriasis
0.700 1.000 1 2016 2016
dbSNP: rs3118471
rs3118471
0.827 0.120 10 6060794 intron variant A/G snv 0.24
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.700 1.000 1 2016 2016
dbSNP: rs2476491
rs2476491
0.776 0.240 10 6053447 intron variant A/T snv 0.25
Juvenile pauciarticular chronic arthritis
0.700 1.000 1 2013 2013
dbSNP: rs2476491
rs2476491
0.776 0.240 10 6053447 intron variant A/T snv 0.25
Systemic onset juvenile chronic arthritis
0.700 1.000 1 2013 2013
dbSNP: rs2476491
rs2476491
0.776 0.240 10 6053447 intron variant A/T snv 0.25
CUI: C0087031
Disease: Juvenile-Onset Still Disease
Juvenile-Onset Still Disease
0.700 1.000 1 2013 2013
dbSNP: rs2476491
rs2476491
0.776 0.240 10 6053447 intron variant A/T snv 0.25
Rheumatoid Arthritis, Systemic Juvenile
0.700 1.000 1 2013 2013
dbSNP: rs2476491
rs2476491
0.776 0.240 10 6053447 intron variant A/T snv 0.25
Oligoarticular Juvenile Idiopathic Arthritis
0.700 1.000 1 2013 2013
dbSNP: rs2476491
rs2476491
0.776 0.240 10 6053447 intron variant A/T snv 0.25
Polyarticular Juvenile Idiopathic Arthritis, Rheumatoid Factor Negative
0.700 1.000 1 2013 2013
dbSNP: rs3118469
rs3118469
10 6059166 intron variant A/T snv 0.24
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
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: 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: 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: rs9663421
rs9663421
1.000 0.080 10 6013641 intron variant C/A;T snv
CUI: C0004096
Disease: Asthma
Asthma
0.700 1.000 1 2019 2019
dbSNP: rs706778
rs706778
0.695 0.320 10 6056986 intron variant C/T snv 0.46
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.800 1.000 3 2010 2019
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: 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: rs61839660
rs61839660
0.776 0.280 10 6052734 intron variant C/T snv 5.7E-02
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.700 1.000 2 2016 2017