Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4833095
TLR1
0.662 0.480 4 38798089 missense variant T/C snv 0.38 0.44 1
rs1041981
LOC100287329 ; LTA
0.667 0.520 6 31573007 missense variant C/A snv 0.35 0.38 2
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67 17
rs4246215
FADS2 ; FEN1
0.677 0.320 11 61796827 3 prime UTR variant G/C;T snv 6
rs1800947
CRP
0.683 0.440 1 159713648 splice region variant C/A;G;T snv 4.4E-05; 5.1E-02; 4.0E-06 1
rs6822844 0.689 0.520 4 122588266 regulatory region variant G/T snv 0.10 5
rs744166
STAT3
0.689 0.560 17 42362183 intron variant A/G snv 0.48 3
rs7517847
IL23R ; C1orf141
0.689 0.600 1 67215986 intron variant T/G snv 0.37 2
rs706778
IL2RA
0.695 0.320 10 6056986 intron variant C/T snv 0.46 4
rs72928038
BACH2
0.695 0.360 6 90267049 intron variant G/A snv 0.11 1
rs917997 0.701 0.480 2 102454108 downstream gene variant T/A;C snv 6
rs12232497 0.701 0.360 17 39883866 intergenic variant T/C snv 0.35 3
rs174537
TMEM258 ; MYRF
0.708 0.400 11 61785208 non coding transcript exon variant G/T snv 0.28 5
rs2201841
C1orf141 ; IL23R
0.716 0.440 1 67228519 intron variant A/G;T snv 4
rs2066847
NOD2
0.716 0.400 16 50729868 frameshift variant C/-;CC delins 1.5E-02 2
rs4246905
TNFSF15
0.716 0.400 9 114790969 missense variant T/A;C snv 0.76 2
rs4676410
GPR35
0.716 0.240 2 240624322 intron variant G/A snv 0.26 1
rs602662
LOC105447645 ; FUT2
0.716 0.280 19 48703728 missense variant G/A snv 0.40 0.47 1
rs7725052 0.716 0.240 5 40487168 intron variant C/T snv 0.52 1
rs7731626
ANKRD55
0.716 0.240 5 56148856 intron variant G/A snv 0.30 1
rs9275572 0.724 0.360 6 32711222 upstream gene variant A/G;T snv 9
rs2111485 0.724 0.280 2 162254026 regulatory region variant A/G snv 0.46 2
rs10174238
STAT4
0.724 0.200 2 191108308 intron variant G/A snv 0.70 1
rs2155219 0.732 0.280 11 76588150 upstream gene variant G/T snv 0.52 7
rs3197999
MST1 ; APEH
0.732 0.280 3 49684099 missense variant G/A snv 0.26 0.27 6