Source: GWASCAT ×
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: rs1801274
rs1801274
FCGR2A
7 0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 0.850 1.000 4 2009 2018
dbSNP: rs10758669
rs10758669 		6 0.763 0.280 9 4981602 upstream gene variant C/A;T snv 0.830 1.000 3 2010 2016
dbSNP: rs11150589
rs11150589
ITGAL
2 1.000 0.040 16 30471173 upstream gene variant T/A;C;G snv 0.800 1.000 3 2012 2017
dbSNP: rs12942547
rs12942547
STAT3
6 0.807 0.200 17 42375526 intron variant A/G;T snv 0.700 1.000 3 2015 2017
dbSNP: rs1728785
rs1728785
ZFP90
1 0.925 0.120 16 68557327 intron variant A/C;T snv 0.77; 7.8E-06 0.810 1.000 3 2009 2017
dbSNP: rs4246905
rs4246905
TNFSF15
15 0.716 0.400 9 114790969 missense variant T/A;C snv 0.76 0.800 1.000 3 2011 2015
dbSNP: rs4380874
rs4380874 		2 1.000 0.040 7 107839870 intergenic variant T/A;C;G snv 0.800 1.000 3 2012 2017
dbSNP: rs4845604
rs4845604
RORC
10 0.776 0.200 1 151829204 intron variant G/A;C;T snv 0.700 1.000 3 2015 2017
dbSNP: rs56167332
rs56167332 		6 0.807 0.160 5 159400761 intron variant C/A;T snv 0.700 1.000 3 2015 2017
dbSNP: rs798502
rs798502
GNA12 ; AMZ1
4 1.000 0.040 7 2750246 intron variant A/C;G snv 0.800 1.000 3 2011 2017
dbSNP: rs10800309
rs10800309 		2 0.925 0.120 1 161502368 upstream gene variant A/G;T snv 0.800 1.000 2 2010 2015
dbSNP: rs11230563
rs11230563
CD6 ; LOC105369326
6 0.790 0.360 11 61008737 missense variant C/G;T snv 4.2E-06; 0.31 0.700 1.000 2 2015 2016
dbSNP: rs11676348
rs11676348 		5 0.790 0.160 2 218145423 regulatory region variant C/G;T snv 0.810 1.000 2 2011 2016
dbSNP: rs11742570
rs11742570 		3 0.925 0.040 5 40410482 upstream gene variant T/C;G snv 0.700 1.000 2 2015 2017
dbSNP: rs12720356
rs12720356
TYK2
7 0.752 0.360 19 10359299 missense variant A/C;G snv 6.1E-02; 4.0E-06 0.700 1.000 2 2015 2016
dbSNP: rs17229285
rs17229285
LOC105373831
2 1.000 0.040 2 198658398 intron variant C/A;T snv 0.800 1.000 2 2012 2015
dbSNP: rs4409764
rs4409764 		3 0.925 0.040 10 99524480 upstream gene variant T/A;G snv 0.700 1.000 2 2015 2017
dbSNP: rs4812833
rs4812833
LINC01620
5 0.827 0.120 20 44440356 intron variant G/A;C snv 0.700 1.000 2 2015 2016
dbSNP: rs661054
rs661054
NXPE1 ; NXPE2
5 0.827 0.120 11 114559688 intron variant A/G;T snv 0.700 1.000 2 2015 2016
dbSNP: rs7282490
rs7282490
GATD3A
4 0.882 0.080 21 44195858 intron variant G/A;T snv 0.700 1.000 2 2015 2017
dbSNP: rs7556897
rs7556897 		6 0.807 0.120 2 227795396 intergenic variant C/G;T snv 0.700 1.000 2 2015 2016
dbSNP: rs9268877
rs9268877
HLA-DRB9
1 0.827 0.200 6 32463370 intron variant A/G;T snv 0.810 1.000 2 2008 2018
dbSNP: rs1001007
rs1001007
CCR5AS
5 0.827 0.120 3 46387167 intron variant A/G;T snv 0.700 1.000 1 2016 2016
dbSNP: rs10010325
rs10010325
TET2 ; TET2-AS1
3 1.000 0.040 4 105185196 intron variant C/A;G;T snv 0.700 1.000 1 2015 2015
dbSNP: rs1004234
rs1004234
IRF1-AS1 ; LINC02863
5 0.827 0.120 5 132421409 intron variant A/G;T snv 0.700 1.000 1 2016 2016