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: 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: rs6679677
rs6679677
0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.800 1.000 2 2008 2015
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: rs9271366
rs9271366
0.807 0.240 6 32619077 intergenic variant G/A snv 0.86
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.820 1.000 2 2011 2015
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: rs9292777
rs9292777
0.925 0.120 5 40437846 regulatory region variant C/T snv 0.60
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.800 1.000 2 2007 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: rs1002922
rs1002922
1.000 0.040 5 40386453 regulatory region variant T/C snv 0.29
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.700 1.000 1 2007 2007
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
dbSNP: rs10114470
rs10114470
0.882 0.080 9 114785492 3 prime UTR variant T/A;C snv
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.710 1.000 1 2013 2014
dbSNP: rs10117785
rs10117785
1.000 0.040 9 114789323 3 prime UTR variant T/A snv 0.34
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.700 1.000 1 2005 2005
dbSNP: rs10181042
rs10181042
1.000 0.040 2 60997124 intron variant C/T snv 0.41
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.800 1.000 1 2010 2010
dbSNP: rs10210302
rs10210302
1.000 0.040 2 233250193 intron variant C/A;T snv
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.810 1.000 1 2007 2010
dbSNP: rs102275
rs102275
0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.810 1.000 1 2010 2018
dbSNP: rs10484545
rs10484545
1.000 0.040 6 29266733 intron variant C/A;G snv
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.700 1.000 1 2007 2007
dbSNP: rs10486483
rs10486483
1.000 0.040 7 26852821 intron variant G/A snv 0.21
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.800 1.000 1 2012 2015
dbSNP: rs10489276
rs10489276
1.000 0.040 1 172893799 intron variant C/T snv 0.31
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.700 1.000 1 2008 2008
dbSNP: rs10489629
rs10489629
0.827 0.240 1 67222666 intron variant T/C snv 0.48
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.700 1.000 1 2006 2006
dbSNP: rs10495903
rs10495903
1.000 0.040 2 43579779 intron variant C/T snv 0.13
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.800 1.000 1 2010 2017
dbSNP: rs10512734
rs10512734
1.000 0.040 5 40393503 intergenic variant A/C;G snv 0.29
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.700 1.000 1 2007 2007
dbSNP: rs1063355
rs1063355
0.827 0.320 6 32659937 3 prime UTR variant T/G snv 0.56
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.700 1.000 1 2013 2013
dbSNP: rs10734105
rs10734105
1.000 0.040 10 131373856 intergenic variant G/A;C;T snv
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.800 1.000 1 2012 2012
dbSNP: rs10761659
rs10761659
0.925 0.040 10 62685804 intron variant A/G snv 0.43
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.810 1.000 1 2010 2017