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: 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: 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: 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: 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: 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: 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: 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: 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: rs4372078
rs4372078
1.000 0.040 9 114801407 intron variant T/G snv 0.78
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.700 1.000 1 2005 2005
dbSNP: rs4574921
rs4574921
0.882 0.160 9 114776054 upstream gene variant C/T snv 0.80
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.700 1.000 1 2005 2005
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: rs1105267
rs1105267
1.000 0.040 13 20365097 intergenic variant G/A snv 0.54
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.700 1.000 1 2006 2006
dbSNP: rs7539328
rs7539328
1.000 0.040 1 67266920 downstream gene variant G/A;T snv
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.700 1.000 1 2006 2006
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: 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: 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: 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: rs10789230
rs10789230
1.000 0.040 1 67264945 downstream gene variant G/C;T snv
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.800 1.000 1 2007 2007
dbSNP: rs10801047
rs10801047
1.000 0.040 1 191590226 intergenic variant A/T snv 0.82
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.800 1.000 1 2007 2007
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: rs1109863
rs1109863
1.000 0.040 16 50658453 intergenic variant G/A snv 0.69
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.700 1.000 1 2007 2007
dbSNP: rs11208994
rs11208994
1.000 0.040 1 67059360 regulatory region variant A/G;T snv
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.700 1.000 1 2007 2007
dbSNP: rs11209002
rs11209002
1.000 0.040 1 67124778 intron variant T/C snv 0.77
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.800 1.000 1 2007 2007
dbSNP: rs11209003
rs11209003
1.000 0.040 1 67135449 intron variant G/T snv 0.28
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.800 1.000 1 2007 2007
dbSNP: rs11209008
rs11209008
0.882 0.080 1 67157615 intron variant G/A;T snv 5.7E-02
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.700 1.000 1 2007 2007