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: rs11209026
rs11209026
0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.900 0.944 6 2006 2020
dbSNP: rs11209026
rs11209026
0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis
0.900 1.000 3 2008 2018
dbSNP: rs11209026
rs11209026
0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis
0.900 1.000 3 2007 2020
dbSNP: rs11209026
rs11209026
0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02
CUI: C0033860
Disease: Psoriasis
Psoriasis
0.900 0.857 2 2008 2018
dbSNP: rs11209026
rs11209026
0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases
0.900 0.773 2 2006 2020
dbSNP: rs7517847
rs7517847
0.689 0.600 1 67215986 intron variant T/G snv 0.37
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.880 1.000 3 2007 2019
dbSNP: rs1004819
rs1004819
0.776 0.360 1 67204530 intron variant G/A snv 0.30
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.860 1.000 1 2006 2019
dbSNP: rs76418789
rs76418789
0.882 0.080 1 67182913 missense variant G/A snv 7.3E-03 4.5E-03
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.850 1.000 2 2011 2019
dbSNP: rs10889677
rs10889677
0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.850 1.000 1 2006 2020
dbSNP: rs2201841
rs2201841
0.716 0.440 1 67228519 intron variant A/G;T snv
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.850 1.000 1 2006 2013
dbSNP: rs2201841
rs2201841
0.716 0.440 1 67228519 intron variant A/G;T snv
CUI: C0033860
Disease: Psoriasis
Psoriasis
0.830 1.000 1 2009 2016
dbSNP: rs10889677
rs10889677
0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis
0.820 1.000 1 2009 2020
dbSNP: rs2201841
rs2201841
0.716 0.440 1 67228519 intron variant A/G;T snv
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis
0.820 1.000 1 2010 2017
dbSNP: rs11805303
rs11805303
0.827 0.240 1 67209833 intron variant C/T snv 0.30
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.810 1.000 1 2007 2012
dbSNP: rs11465804
rs11465804
0.752 0.320 1 67236843 intron variant T/G snv 4.4E-02 5.4E-02
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.800 1.000 3 2006 2010
dbSNP: rs10889676
rs10889676
0.827 0.120 1 67256884 intron variant C/A;T snv
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.800 1.000 2 2007 2016
dbSNP: rs11465802
rs11465802
1.000 0.040 1 67219915 intron variant A/C;T snv
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.800 1.000 1 2007 2007
dbSNP: rs1343151
rs1343151
0.752 0.400 1 67253446 intron variant G/A snv 0.41
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.800 1.000 1 2006 2007
dbSNP: rs2064689
rs2064689
1.000 0.040 1 67187327 intron variant G/A snv 0.29
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.800 1.000 1 2007 2007
dbSNP: rs2902440
rs2902440
1.000 0.040 1 67205233 intron variant G/A snv 0.37
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.800 1.000 1 2007 2007
dbSNP: rs9988642
rs9988642
0.882 0.080 1 67260421 downstream gene variant T/C snv 0.13
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.800 1.000 1 2007 2007
dbSNP: rs9988642
rs9988642
0.882 0.080 1 67260421 downstream gene variant T/C snv 0.13
CUI: C0033860
Disease: Psoriasis
Psoriasis
0.800 1.000 1 2012 2012
dbSNP: rs7517847
rs7517847
0.689 0.600 1 67215986 intron variant T/G snv 0.37
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis
0.730 1.000 1 2008 2016
dbSNP: rs7517847
rs7517847
0.689 0.600 1 67215986 intron variant T/G snv 0.37
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis
0.720 1.000 1 2012 2018
dbSNP: rs117633859
rs117633859
1.000 0.120 1 67162145 intron variant A/G snv 2.6E-02
CUI: C0042170
Disease: Uveomeningoencephalitic Syndrome
Uveomeningoencephalitic Syndrome
0.710 1.000 1 2014 2014