Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6556756
LOC105377703 ; LINC02143
0.882 0.160 5 164462274 intron variant G/T snv 0.89 2
rs4242384 0.882 0.160 8 127506309 regulatory region variant C/A snv 0.88 2
rs169111
ITGA9
1.000 0.120 3 37474042 intron variant C/T snv 0.84 1
rs1465618
THADA
0.882 0.160 2 43326810 intron variant T/C snv 0.80 2
rs2660753 0.790 0.240 3 87061524 intergenic variant T/C snv 0.76 2
rs5009448
HLA-A
1.000 0.120 6 29972711 upstream gene variant T/C snv 0.74 1
rs2180341
RNF146
0.882 0.160 6 127279485 intron variant G/A snv 0.73 2
rs3802842
COLCA2 ; COLCA1
0.695 0.280 11 111300984 intron variant C/A snv 0.71 2
rs10821936
ARID5B
0.742 0.200 10 61963818 intron variant C/T snv 0.69 2
rs1800871
IL19 ; IL10
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 1
rs3095341 1.000 0.120 6 30758971 intron variant T/C snv 0.69 1
rs651164
SLC22A1
0.882 0.160 6 160160342 downstream gene variant A/G snv 0.69 2
rs889312 0.732 0.360 5 56736057 regulatory region variant C/A snv 0.69 2
rs4779584 0.732 0.160 15 32702555 intergenic variant T/C snv 0.67 2
rs995030
KITLG
0.776 0.320 12 88496894 3 prime UTR variant A/G snv 0.67 4
rs7176508
DRAIC
0.851 0.280 15 69726651 intron variant A/G snv 0.67 3
rs417162
HLA-A
1.000 0.120 6 29948728 downstream gene variant C/T snv 0.66 2
rs6457327 0.790 0.320 6 31106253 downstream gene variant A/C snv 0.66 3
rs4474514
KITLG
0.827 0.240 12 88560182 intron variant G/A snv 0.65 2
rs4977756
CDKN2B-AS1
0.683 0.440 9 22068653 intron variant G/A snv 0.64 5
rs7014346
CASC8 ; POU5F1B ; PCAT1
0.732 0.240 8 127412547 intron variant A/G snv 0.63 3
rs3803662
CASC16
0.662 0.440 16 52552429 non coding transcript exon variant A/G snv 0.63 3
rs9260484
HLA-A
1.000 0.120 6 29952476 upstream gene variant A/C snv 0.62 1
rs6939340
CASC15 ; NBAT1
0.851 0.160 6 22139775 intron variant A/G snv 0.62 2
rs2191566
ZNF230
0.925 0.200 19 44007237 intron variant G/T snv 0.62 2