Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1734907 0.925 0.080 7 100717894 upstream gene variant A/G snv 0.84 1
rs314313
EPHB4 ; SLC12A9
1.000 0.040 7 100825743 intron variant T/A;C;G snv 0.29 2
rs503734
IMPG2
1.000 0.040 3 101304904 intron variant A/G snv 0.40 2
rs13107612
BANK1
0.827 0.120 4 101818823 intron variant C/T snv 0.31 5
rs13126505
BANK1
1.000 0.040 4 101944147 intron variant G/A snv 4.1E-02 3
rs34592089
BANK1
1.000 0.040 4 102005766 intron variant G/A;T snv 2
rs4851529
LOC107985926
0.827 0.120 2 102030838 downstream gene variant G/A snv 0.44 5
rs10185424 0.925 0.040 2 102046427 intron variant T/G snv 0.62 2
rs871656
IL1R1
0.827 0.120 2 102154822 intron variant T/A;C snv 5
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 24
rs13001325
IL18R1 ; IL1RL1
1.000 0.040 2 102322576 intron variant C/T snv 0.30 2
rs13015714
IL18R1
0.882 0.200 2 102355405 intron variant G/T snv 0.77 2
rs12987977
IL18R1
0.827 0.120 2 102358876 intron variant T/G snv 0.31 5
rs2058660
IL18RAP
0.882 0.280 2 102437989 intron variant G/A snv 0.78 1
rs6708413
IL18RAP
1.000 0.040 2 102446909 intron variant G/A snv 0.78 2
rs917997 0.701 0.480 2 102454108 downstream gene variant T/A;C snv 2
rs2075184 0.724 0.240 2 102464132 intergenic variant T/C snv 0.78 14
rs3774937
NFKB1
0.776 0.280 4 102513096 intron variant T/C snv 0.26 5
rs230534
NFKB1
0.882 0.120 4 102527884 intron variant T/C snv 0.73 2
rs7705924
LINC00492 ; LINC00491
1.000 0.040 5 102611094 intron variant A/G snv 5.1E-02 1
rs5498
ICAM4 ; ICAM1
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 2
rs74956615
FDX2 ; RAVER1
0.807 0.160 19 10317045 3 prime UTR variant T/A;C snv 5
rs35018800
TYK2
0.790 0.160 19 10354167 missense variant G/A snv 4.6E-03 4.9E-03 5
rs12720356
TYK2
0.752 0.360 19 10359299 missense variant A/C;G snv 6.1E-02; 4.0E-06 7
rs280519
TYK2
0.752 0.320 19 10362257 splice region variant A/C;G snv 0.50 1