Source: GWASDB

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: rs2076756
rs2076756
0.882 0.040 16 50722970 intron variant A/G snv 0.17
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.830 1.000 6 2007 2019
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 4 2006 2010
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 3 2006 2007
dbSNP: rs1893217
rs1893217
0.742 0.440 18 12809341 intron variant A/G snv 0.12
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.850 1.000 3 2008 2016
dbSNP: rs212388
rs212388
0.827 0.240 6 159069404 intron variant C/G;T snv
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.810 1.000 3 2010 2017
dbSNP: rs10045431
rs10045431
0.851 0.240 5 159387525 intron variant A/C snv 0.78
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.810 1.000 2 2008 2014
dbSNP: rs10188217
rs10188217
0.925 0.080 2 60990407 intron variant T/A;C snv
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.800 1.000 2 2008 2011
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 2 2007 2012
dbSNP: rs13003464
rs13003464
0.827 0.200 2 60959694 intron variant A/G snv 0.50
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.800 1.000 2 2008 2012
dbSNP: rs17221417
rs17221417
0.925 0.040 16 50705671 intron variant C/G snv 0.20
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.810 1.000 2 2007 2017
dbSNP: rs17309827
rs17309827
1.000 0.040 6 3433084 intron variant T/G snv 0.30
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.800 1.000 2 2008 2010
dbSNP: rs1736020
rs1736020
1.000 0.040 21 15440233 intron variant C/A snv 0.33
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.800 1.000 2 2008 2010
dbSNP: rs2024092
rs2024092
0.827 0.120 19 1124032 intron variant G/A snv 0.24 0.26
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.800 1.000 2 2008 2017
dbSNP: rs2188962
rs2188962
0.882 0.160 5 132435113 intron variant C/T snv 0.29
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.810 1.000 2 2008 2017
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 2 2006 2013
dbSNP: rs2301436
rs2301436
0.752 0.320 6 167024500 intron variant C/T snv 0.42
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.810 1.000 2 2008 2016
dbSNP: rs5743289
rs5743289
1.000 0.040 16 50722863 intron variant C/G;T snv
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.810 1.000 2 2007 2014
dbSNP: rs6478108
rs6478108
0.763 0.200 9 114796423 intron variant C/T snv 0.73
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.760 1.000 2 2005 2018
dbSNP: rs6651252
rs6651252
0.790 0.200 8 128554935 intron variant T/C snv 0.19
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.810 1.000 2 2010 2019
dbSNP: rs6908425
rs6908425
0.752 0.320 6 20728500 intron variant T/C snv 0.78
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.800 1.000 2 2008 2015
dbSNP: rs7702331
rs7702331
1.000 0.040 5 73255307 intron variant A/G snv 0.42
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.800 1.000 2 2010 2012
dbSNP: rs9286879
rs9286879
0.851 0.200 1 172893094 intron variant A/G snv 0.32
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.800 1.000 2 2008 2012
dbSNP: rs1000113
rs1000113
0.925 0.040 5 150860514 intron variant C/T snv 0.13
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.840 1.000 1 2007 2015
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: rs10065637
rs10065637
1.000 0.040 5 56143024 intron variant C/T snv 0.15
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.800 1.000 1 2012 2012