Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs16844401
HGFAC
1.000 0.040 4 3447925 missense variant G/A;T snv 7.5E-02; 8.3E-06 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
rs1800789
FGB
1.000 0.040 4 154561591 upstream gene variant G/A snv 0.17 3
rs1800790
FGB
0.851 0.200 4 154562556 upstream gene variant G/A snv 0.15 3
rs1938492 1 65652146 intergenic variant A/C snv 0.43 3
rs2059503
FGB
4 154572267 downstream gene variant A/T snv 0.14 3
rs2070016
FGA
1.000 0.040 4 154589162 intron variant A/G snv 0.12 3
rs2106854
IRF1-AS1
5 132433482 intron variant C/T snv 0.23 3
rs2227421
FGB
4 154571072 3 prime UTR variant A/C snv 0.26 3
rs2286503
TOMM7
7 22816987 intron variant C/T snv 0.48 3
rs2522056
IRF1-AS1
5 132466034 intron variant G/A snv 0.25 3
rs270607
MIR3936HG ; SLC22A4
5 132313493 intron variant A/G snv 0.69 3
rs3091307
TH2LCRR
0.925 0.160 5 132653444 intron variant A/G snv 0.34 3
rs4220
FGB
0.925 0.080 4 154570607 missense variant G/A snv 0.17 0.15 3
rs434943 14 68847342 intergenic variant G/A snv 0.27 3
rs4463047 4 154574381 downstream gene variant T/C snv 0.15 3
rs4508864 4 154560137 upstream gene variant C/G;T snv 3
rs4817986 21 39093586 regulatory region variant G/T snv 0.22 3
rs4925659
NLRP3
1 247440161 intron variant G/A snv 0.33 3
rs511154 3 136232079 intergenic variant A/G;T snv 3