Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs113612868
TCAP
1.000 0.080 17 39665182 upstream gene variant -/T ins 1
rs10045431 0.851 0.240 5 159387525 intron variant A/C snv 0.78 3
rs1054609
ZPBP2
0.925 0.160 17 39877024 3 prime UTR variant A/C snv 0.40 2
rs11167764
LOC105378204
0.925 0.120 5 142099500 regulatory region variant A/C snv 0.80 2
rs1342326 0.790 0.360 9 6190076 intergenic variant A/C snv 0.21 2
rs3129878
HLA-DRA
0.807 0.360 6 32440958 intron variant A/C snv 0.30 2
rs9378805 0.851 0.280 6 417727 intergenic variant A/C snv 0.36 2
rs10455025
TSLP
1.000 0.080 5 111069301 upstream gene variant A/C snv 0.24 1
rs11048311 1.000 0.080 12 25869205 downstream gene variant A/C snv 0.18 1
rs1538084 1.000 0.080 1 152523536 intergenic variant A/C snv 0.79 1
rs3135499
NOD2
0.882 0.160 16 50732216 splice donor variant A/C snv 0.45 1
rs7086533
LINC02660
1.000 0.080 10 3926521 intron variant A/C snv 0.91 1
rs7219080
GSDMA
1.000 0.080 17 39958263 intron variant A/C snv 0.65 1
rs9268644
HLA-DRA
0.827 0.360 6 32440267 intron variant A/C snv 0.68 1
rs1250552
ZMIZ1
0.882 0.200 10 79298270 intron variant A/C;G snv 5
rs13010713
LINC01934
0.882 0.200 2 181131318 intron variant A/C;G snv 5
rs1801274
FCGR2A
0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 5
rs9792269 0.882 0.200 8 128252343 intergenic variant A/C;G snv 5
rs6010620
RTEL1 ; RTEL1-TNFRSF6B
0.701 0.360 20 63678486 intron variant A/C;G snv 4
rs17498196
LOC107987046 ; IL33
1.000 0.080 9 6237547 intron variant A/C;G snv 2
rs241425
TAP2
0.925 0.160 6 32837132 intron variant A/C;G snv 2
rs2538026 1.000 0.080 18 56261410 intergenic variant A/C;G snv 1
rs1229598 1.000 0.080 18 56267556 regulatory region variant A/C;G;T snv 1
rs2228145
IL6R
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 5
rs1412426 1.000 0.080 9 6188652 intergenic variant A/C;T snv 1