Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2647046 0.882 0.200 6 32700559 TF binding site variant A/C snv 0.64 3
rs2858884 0.925 0.200 6 32732306 upstream gene variant A/C snv 0.23 2
rs9270986
HLA-DRB1
0.882 0.160 6 32606283 intergenic variant A/C snv 0.85 2
rs10160659
DCHS1
1.000 0.080 11 6644463 intron variant A/C snv 5.5E-02 1
rs17044542 1.000 0.080 3 6299812 intron variant A/C snv 5.2E-02 1
rs2839750
LOC105369165
1.000 0.080 2 52901952 intron variant A/C snv 3.1E-02 1
rs7175718
ADAMTSL3
0.882 0.120 15 83900350 intron variant A/C snv 1.6E-02 1
rs7187262
CYB5B
1.000 0.080 16 69460376 intron variant A/C snv 0.11 1
rs7579759
PLB1
1.000 0.080 2 28470781 intron variant A/C snv 0.42 1
rs9373298 1.000 0.080 6 141198693 regulatory region variant A/C snv 0.27 1
rs10226621
SDK1
1.000 0.080 7 4068008 intron variant A/C;G snv 1
rs17138435 0.882 0.120 11 79481943 TF binding site variant A/C;G snv 1.6E-02 1
rs686881
POLI
1.000 0.080 18 54287164 intron variant A/C;G snv 1
rs7105164
MICAL2
1.000 0.080 11 12132546 intron variant A/C;G snv 5.0E-02 1
rs6023560 0.882 0.120 20 54743554 intergenic variant A/C;G;T snv 0.12 1
rs539703
TSBP1-AS1 ; TSBP1
0.882 0.200 6 32320685 intron variant A/C;T snv 4
rs9267954 0.882 0.200 6 32245275 regulatory region variant A/C;T snv 3
rs10775354
RBFOX1
1.000 0.080 16 6757689 intron variant A/C;T snv 1
rs2239800
HLA-DQA2
0.882 0.280 6 32745490 intron variant A/G snv 0.11 3
rs9275418 0.882 0.200 6 32702467 downstream gene variant A/G snv 0.30 3
rs2227127
HLA-DQA2
0.925 0.120 6 32744005 intron variant A/G snv 0.37 2
rs10091183 1.000 0.080 8 33215980 regulatory region variant A/G snv 4.6E-02 1
rs1009449
LOC105376617
1.000 0.080 11 33684620 intron variant A/G snv 4.2E-03 1
rs10956273
LINC00861
1.000 0.080 8 125953914 non coding transcript exon variant A/G snv 6.9E-02 1
rs11574049
VDR
1.000 0.080 12 47878732 intron variant A/G snv 1.6E-02 1