Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2428494
HLA-B
0.827 0.160 6 31354420 intron variant T/A;C snv 5
rs9272346
HLA-DQA1
0.790 0.320 6 32636595 intron variant G/A snv 0.54 4
rs9273349
HLA-DQB1-AS1
0.827 0.200 6 32658092 upstream gene variant T/C;G snv 1
rs28407950
HLA-DQB1-AS1
0.925 0.080 6 32658571 upstream gene variant C/T snv 0.29 2
rs4491851
GLB1
0.925 0.080 3 33042493 intron variant G/A snv 0.50 2
rs10414065 0.882 0.080 19 33230549 upstream gene variant C/T snv 5.5E-02 4
rs117710327 0.882 0.080 19 33235672 TF binding site variant C/A snv 5.0E-02 5
rs11088309
RUNX1
0.925 0.080 21 35092334 intron variant C/A;G snv 9.3E-02 2
rs11742240 0.925 0.080 5 35881274 downstream gene variant G/A;T snv 2
rs190438685 0.925 0.080 4 39388825 intergenic variant C/T snv 6.2E-03 2
rs28635831
COG6
0.925 0.080 13 39745817 intron variant A/G snv 0.27 2
rs7216389
GSDMB
0.732 0.440 17 39913696 intron variant C/T snv 0.60 1
rs2544026
HDAC7
0.925 0.080 12 47792780 non coding transcript exon variant T/A snv 0.19 2
rs56389811
HDAC7
1.000 12 47811575 intron variant C/A;T snv 1
rs10667251 0.925 0.080 17 49388381 intron variant -/TCT delins 0.47 4
rs705699
SUOX ; RAB5B
0.882 0.160 12 55991020 non coding transcript exon variant G/A snv 0.40 5
rs7302200 0.851 0.200 12 56055651 regulatory region variant G/A snv 0.23 6
rs1059513
NAB2 ; STAT6
0.776 0.240 12 57095926 3 prime UTR variant T/C snv 8.0E-02 6
rs3122929
STAT6
0.882 0.080 12 57115319 intron variant C/T snv 0.33 4
rs62557312 0.925 0.080 9 6047765 intron variant C/T snv 0.15 2
rs12722502
IL2RA
0.882 0.080 10 6051176 intron variant C/T snv 7.8E-03 4
rs7183955
RORA
0.925 0.080 15 60757370 intron variant A/C snv 0.24 2
rs174535
MYRF ; TMEM258
0.776 0.280 11 61783884 missense variant T/A;C;G snv 0.38 0.32 11
rs174621
FADS2
1.000 11 61862632 non coding transcript exon variant G/A;C snv 1
rs1342326 0.790 0.360 9 6190076 intergenic variant A/C snv 0.21 2