Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2066861
FGG
4 154606284 intron variant C/T snv 0.26 5
rs4129267
IL6R
0.807 0.200 1 154453788 intron variant C/G;T snv 5
rs7681423 4 154621096 intergenic variant C/T snv 0.26 5
rs12239046
NLRP3
1 247438293 intron variant T/C snv 0.58 4
rs2073643
SLC22A5
1.000 0.080 5 132387596 intron variant T/C snv 0.46 4
rs2158177
TH2LCRR
0.925 0.120 5 132648366 intron variant A/G snv 0.18 4
rs4537545
IL6R
0.790 0.160 1 154446403 intron variant C/T snv 0.48 4
rs6734238 1.000 0.080 2 113083453 upstream gene variant A/G snv 0.39 4
rs7529229
IL6R
0.851 0.120 1 154448302 intron variant T/C snv 0.48 4
rs10034922 4 154599476 downstream gene variant G/A snv 5.2E-02 3
rs10157379
NLRP3
1 247442297 intron variant C/G;T snv 3
rs1016988 5 132408882 upstream gene variant T/C snv 0.20 3
rs10226084 7 17957989 upstream gene variant T/C snv 0.46 3
rs10512597
RAB37 ; CD300LF
17 74703694 intron variant T/A;C snv 3
rs11242111
LINC02863 ; IRF1-AS1
5 132420366 intron variant A/G;T snv 3
rs1154988 3 136206349 upstream gene variant T/A snv 0.76 3
rs12511469 4 154530607 downstream gene variant T/A snv 0.18 3
rs12651106
DCHS2
4 154379907 intron variant C/A snv 0.12 3
rs12712127
IL1R1
2 102110201 intron variant A/G snv 0.62 3
rs12915708
SPPL2A
15 50756405 intron variant G/A;C snv 3
rs1476698
FARP2
2 241357034 intron variant A/G;T snv 3
rs1539019
NLRP3
0.882 0.240 1 247436999 intron variant A/C snv 0.63 3
rs17690122 5 132532143 intron variant A/G;T snv 3
rs1800787
FGB
1.000 0.040 4 154562863 upstream gene variant C/T snv 0.17 3
rs1800788
FGB
4 154562762 upstream gene variant C/T snv 0.18 3