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: rs2006996
rs2006996
0.882 0.080 9 114830358 regulatory region variant T/C snv 7.2E-02
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.800 1.000 1 2011 2013
dbSNP: rs16931910
rs16931910
1.000 0.040 9 114856029 intron variant A/C snv 7.2E-02
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.700 1.000 1 2005 2005
dbSNP: rs4979467
rs4979467
0.925 0.080 9 114867763 intron variant C/T snv 0.52
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.700 1.000 1 2013 2013
dbSNP: rs7863183
rs7863183
0.925 0.080 9 114880138 intron variant T/A;C snv
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.700 1.000 1 2013 2013
dbSNP: rs2974
rs2974
1.000 0.040 9 114901892 intron variant T/C snv 0.56
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.700 1.000 1 2005 2005
dbSNP: rs2295800
rs2295800
1.000 0.040 9 114901931 intron variant T/C snv 0.56
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.700 1.000 1 2005 2005
dbSNP: rs3181362
rs3181362
1.000 0.040 9 114905163 intron variant T/C snv 0.21
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.700 1.000 1 2013 2013
dbSNP: rs1322054
rs1322054
1.000 0.040 9 114907019 intron variant A/G snv 0.58
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.700 1.000 1 2005 2005
dbSNP: rs3789882
rs3789882
1.000 0.040 9 114907419 intron variant A/T snv 0.22
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.700 1.000 1 2005 2005
dbSNP: rs3789879
rs3789879
1.000 0.040 9 114915956 intron variant T/C snv 0.58
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.700 1.000 1 2005 2005
dbSNP: rs1885383
rs1885383
1.000 0.040 9 114917522 intron variant G/A snv 0.21
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.700 1.000 1 2005 2005
dbSNP: rs3181360
rs3181360
1.000 0.040 9 114929278 intron variant C/A;T snv
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.700 1.000 1 2013 2013
dbSNP: rs254079
rs254079
1.000 0.040 5 116555387 intron variant A/G snv 0.49
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.700 1.000 1 2008 2008
dbSNP: rs495662
rs495662
1.000 0.040 6 117802987 intergenic variant G/A snv 0.92
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.700 1.000 1 2008 2008
dbSNP: rs10886462
rs10886462
1.000 0.040 10 119345799 intron variant A/G snv 0.22
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.700 1.000 1 2007 2007
dbSNP: rs3897478
rs3897478
1.000 0.040 1 119908567 downstream gene variant T/C snv 0.17
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.800 1.000 1 2012 2012
dbSNP: rs921720
rs921720
1.000 0.040 8 125522429 intron variant A/G snv 0.48
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.800 1.000 1 2008 2017
dbSNP: rs4871611
rs4871611
1.000 0.040 8 125525328 intron variant G/A snv 0.48
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.800 1.000 1 2010 2010
dbSNP: rs1551398
rs1551398
0.882 0.160 8 125527809 intron variant G/A snv 0.48
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.800 1.000 1 2008 2008
dbSNP: rs9491697
rs9491697
1.000 0.040 6 127134977 intron variant A/G snv 0.41
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.800 1.000 1 2012 2017
dbSNP: rs226534
rs226534
1.000 0.040 X 127768516 intergenic variant A/G snv 0.34
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.700 1.000 1 2008 2008
dbSNP: rs2542151
rs2542151
0.763 0.480 18 12779948 upstream gene variant G/T snv 0.83
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.880 1.000 4 2007 2016
dbSNP: rs13204742
rs13204742
1.000 0.040 6 127924620 intergenic variant G/T snv 9.3E-02
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.800 1.000 1 2012 2012
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: rs657555
rs657555
0.925 0.080 18 12847137 intron variant C/A;T snv
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.700 1.000 1 2011 2011