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: rs2104286
rs2104286
0.692 0.321 10 6057082 intron variant T/C snp 0.18
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.870 1.000 2 2007 2015
dbSNP: rs12722489
rs12722489
0.878 0.143 10 6060049 intron variant C/T snp 0.11
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.830 1.000 2 2007 2012
dbSNP: rs12722515
rs12722515
1.000 0.036 10 6039267 intron variant C/A snp 0.13
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases
0.800 2 2012 2016
dbSNP: rs3118470
rs3118470
0.744 0.321 10 6059750 intron variant T/A,C snp 6.1E-04; 0.31
CUI: C0002171
Disease: Alopecia Areata
Alopecia Areata
0.800 2 2010 2016
dbSNP: rs61839660
rs61839660
0.801 0.214 10 6052734 intron variant C/T snp 5.1E-02
Diabetes Mellitus, Insulin-Dependent
0.800 2 2012 2015
dbSNP: rs706778
rs706778
0.699 0.286 10 6056986 intron variant C/T snp 0.47
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.800 2 2010 2014
dbSNP: rs706779
rs706779
0.846 0.143 10 6056861 intron variant T/C snp 0.46
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.800 2 2010 2017
dbSNP: rs12722495
rs12722495
0.878 0.143 10 6055320 intron variant T/C snp 6.5E-02
Diabetes Mellitus, Insulin-Dependent
0.800 1 2011 2011
dbSNP: rs3118470
rs3118470
0.744 0.321 10 6059750 intron variant T/A,C snp 6.1E-04; 0.31
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.800 1 2011 2011
dbSNP: rs706778
rs706778
0.699 0.286 10 6056986 intron variant C/T snp 0.47
Diabetes Mellitus, Insulin-Dependent
0.750 1.000 1 2007 2016
dbSNP: rs706778
rs706778
0.699 0.286 10 6056986 intron variant C/T snp 0.47
CUI: C0178468
Disease: Autoimmune thyroid disease
Autoimmune thyroid disease
0.710 1.000 1 2010 2015
dbSNP: rs61839660
rs61839660
0.801 0.214 10 6052734 intron variant C/T snp 5.1E-02
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.700 2 2017 2017
dbSNP: rs12253981
rs12253981
1.000 0.071 10 6050383 intron variant T/G snp 0.28
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.700 1 2017 2017
dbSNP: rs12722486
rs12722486
1.000 10 6061799 intron variant C/A,T snp 3.8E-02
CUI: C0031117
Disease: Peripheral Neuropathy
Peripheral Neuropathy
0.700 1 2015 2015
dbSNP: rs12722486
rs12722486
1.000 10 6061799 intron variant C/A,T snp 3.8E-02
CUI: C2363741
Disease: HIV-1 infection
HIV-1 infection
0.700 1 2015 2015
dbSNP: rs12722515
rs12722515
1.000 0.036 10 6039267 intron variant C/A snp 0.13
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.700 1 2016 2016
dbSNP: rs12722561
rs12722561
1.000 0.071 10 6027930 intron variant C/A,T snp 0.15
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.700 1 2016 2016
dbSNP: rs2104286
rs2104286
0.692 0.321 10 6057082 intron variant T/C snp 0.18
CUI: C0008313
Disease: Cholangitis, Sclerosing
Cholangitis, Sclerosing
0.700 1 2017 2017
dbSNP: rs2104286
rs2104286
0.692 0.321 10 6057082 intron variant T/C snp 0.18
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.700 1 2017 2017
dbSNP: rs2104286
rs2104286
0.692 0.321 10 6057082 intron variant T/C snp 0.18
CUI: C0033860
Disease: Psoriasis
Psoriasis
0.700 1 2017 2017
dbSNP: rs2104286
rs2104286
0.692 0.321 10 6057082 intron variant T/C snp 0.18
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis
0.700 1 2017 2017
dbSNP: rs2104286
rs2104286
0.692 0.321 10 6057082 intron variant T/C snp 0.18
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis
0.700 1 2017 2017
dbSNP: rs3118471
rs3118471
0.821 0.107 10 6060794 intron variant A/G snp 0.26
CUI: C0033860
Disease: Psoriasis
Psoriasis
0.700 1 2017 2017
dbSNP: rs3118471
rs3118471
0.821 0.107 10 6060794 intron variant A/G snp 0.26
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis
0.700 1 2017 2017
dbSNP: rs3118471
rs3118471
0.821 0.107 10 6060794 intron variant A/G snp 0.26
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis
0.700 1 2017 2017