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: rs13126505
rs13126505
BANK1
1.000 0.040 4 101944147 intron variant G/A snv 4.1E-02
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.800 1.000 1 2012 2017
dbSNP: rs2058660
rs2058660
IL18RAP
0.882 0.280 2 102437989 intron variant G/A snv 0.78
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.810 1.000 1 2010 2015
dbSNP: rs7705924
rs7705924
LINC00491 ; LINC00492
1.000 0.040 5 102611094 intron variant A/G snv 5.1E-02
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.800 1.000 1 2012 2012
dbSNP: rs12720356
rs12720356
TYK2
0.752 0.360 19 10359299 missense variant A/C;G snv 6.1E-02; 4.0E-06
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.800 1.000 1 2010 2016
dbSNP: rs6568421
rs6568421 		1.000 0.040 6 105987150 regulatory region variant A/G snv 0.23
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.800 1.000 1 2010 2010
dbSNP: rs7746082
rs7746082 		0.851 0.160 6 105987394 regulatory region variant G/A;C snv
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.810 1.000 1 2008 2017
dbSNP: rs11195128
rs11195128 		1.000 0.040 10 110426390 downstream gene variant C/G;T snv
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.810 1.000 1 2014 2017
dbSNP: rs4807569
rs4807569
SBNO2
0.925 0.120 19 1123379 intron variant A/C snv 0.25
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.710 1.000 1 2008 2010
dbSNP: rs2024092
rs2024092
SBNO2
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: rs740495
rs740495
SBNO2
1.000 0.040 19 1124836 intron variant A/C;G snv
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.800 1.000 1 2010 2010
dbSNP: rs6679677
rs6679677
PHTF1
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: rs2476601
rs2476601
PTPN22 ; AP4B1-AS1
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.860 0.800 2 2005 2016
dbSNP: rs12552933
rs12552933 		1.000 0.040 9 114759302 intergenic variant C/T snv 2.9E-02
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.700 1.000 1 2013 2013
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: rs6478106
rs6478106 		0.925 0.080 9 114783386 downstream gene variant C/T snv 0.34
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.820 1.000 2 2005 2019
dbSNP: rs10114470
rs10114470
TNFSF15
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
TNFSF15
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: rs3810936
rs3810936
TNFSF15
0.742 0.320 9 114790605 synonymous variant T/C snv 0.71 0.75
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.850 1.000 2 2005 2018
dbSNP: rs6478108
rs6478108
TNFSF15
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: rs4372078
rs4372078
TNFSF15
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: rs4263839
rs4263839
TNFSF15
0.807 0.160 9 114804160 intron variant A/G snv 0.75
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.830 0.750 1 2008 2014
dbSNP: rs4979462
rs4979462
TNFSF15
0.790 0.240 9 114804733 intron variant C/T snv 0.13
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.720 1.000 1 2005 2016
dbSNP: rs6478109
rs6478109
TNFSF15
0.752 0.320 9 114806486 upstream gene variant A/G snv 0.74
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.830 1.000 3 2005 2016
dbSNP: rs7848647
rs7848647
TNFSF15
0.732 0.320 9 114806766 upstream gene variant T/C snv 0.74
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.840 1.000 1 2005 2018
dbSNP: rs7869487
rs7869487 		0.882 0.040 9 114818634 intergenic variant C/G;T snv
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.830 1.000 1 2005 2015