Source: GWASDB ×
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs7517847
rs7517847
IL23R ; C1orf141
2 0.689 0.600 1 67215986 intron variant T/G snv 0.37 0.880 1.000 1 2007 2019
dbSNP: rs744166
rs744166
STAT3
3 0.689 0.560 17 42362183 intron variant A/G snv 0.48 0.870 1.000 1 2008 2016
dbSNP: rs1004819
rs1004819
IL23R ; C1orf141
1 0.776 0.360 1 67204530 intron variant G/A snv 0.30 0.860 1.000 1 2006 2019
dbSNP: rs3024505
rs3024505 		6 0.790 0.320 1 206766559 upstream gene variant G/A snv 0.11 0.850 0.875 1 2008 2017
dbSNP: rs76418789
rs76418789
IL23R ; C1orf141
1 0.882 0.080 1 67182913 missense variant G/A snv 7.3E-03 4.5E-03 0.850 1.000 1 2011 2019
dbSNP: rs1000113
rs1000113
IRGM
1 0.925 0.040 5 150860514 intron variant C/T snv 0.13 0.840 1.000 1 2007 2015
dbSNP: rs7848647
rs7848647
TNFSF15
1 0.732 0.320 9 114806766 upstream gene variant T/C snv 0.74 0.840 1.000 1 2005 2018
dbSNP: rs4263839
rs4263839
TNFSF15
3 0.807 0.160 9 114804160 intron variant A/G snv 0.75 0.830 0.750 1 2008 2014
dbSNP: rs7869487
rs7869487 		1 0.882 0.040 9 114818634 intergenic variant C/G;T snv 0.830 1.000 1 2005 2015
dbSNP: rs11175593
rs11175593
LRRK2 ; LINC02471 ; LOC105369735 ; LRRK2-DT
3 0.882 0.160 12 40208138 non coding transcript exon variant C/T snv 2.8E-02 0.820 1.000 1 2008 2013
dbSNP: rs11747270
rs11747270
IRGM
3 0.790 0.240 5 150879305 intron variant A/G snv 0.21 0.820 0.667 1 2008 2020
dbSNP: rs1250550
rs1250550
ZMIZ1
3 0.851 0.240 10 79300560 intron variant C/A snv 0.27 0.820 1.000 1 2010 2017
dbSNP: rs4409764
rs4409764 		2 0.925 0.040 10 99524480 upstream gene variant T/A;G snv 0.820 1.000 1 2010 2019
dbSNP: rs10210302
rs10210302
ATG16L1
1 1.000 0.040 2 233250193 intron variant C/A;T snv 0.810 1.000 1 2007 2010
dbSNP: rs102275
rs102275
TMEM258
10 0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47 0.810 1.000 1 2010 2018
dbSNP: rs10761659
rs10761659 		2 0.925 0.040 10 62685804 intron variant A/G snv 0.43 0.810 1.000 1 2010 2017
dbSNP: rs11190140
rs11190140
NKX2-3 ; LINC01475
4 0.827 0.160 10 99531836 upstream gene variant T/C snv 0.55 0.810 1.000 1 2008 2014
dbSNP: rs11195128
rs11195128 		1 1.000 0.040 10 110426390 downstream gene variant C/G;T snv 0.810 1.000 1 2014 2017
dbSNP: rs11235667
rs11235667 		1 0.925 0.120 11 73152652 intergenic variant A/G snv 2.3E-03 0.810 1.000 1 2014 2014
dbSNP: rs11564258
rs11564258
MUC19 ; LOC105369736
2 1.000 0.040 12 40398498 intron variant G/A snv 3.1E-02 0.810 1.000 1 2010 2018
dbSNP: rs12521868
rs12521868
IRF1-AS1
1 1.000 0.040 5 132448701 intron variant G/T snv 0.28 0.810 1.000 1 2010 2012
dbSNP: rs1456893
rs1456893 		3 0.851 0.160 7 50230076 intron variant G/A snv 0.69 0.810 1.000 1 2008 2011
dbSNP: rs2058660
rs2058660
IL18RAP
1 0.882 0.280 2 102437989 intron variant G/A snv 0.78 0.810 1.000 1 2010 2015
dbSNP: rs224136
rs224136 		2 0.925 0.120 10 62710915 intron variant C/A;T snv 0.34 0.810 0.667 1 2007 2019
dbSNP: rs2797685
rs2797685
PER3
1 0.882 0.160 1 7819003 intron variant C/T snv 0.23 0.810 1.000 1 2010 2012