Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3104402 1.000 0.120 6 32713899 upstream gene variant T/G snv 0.96 1
rs4948088 0.925 0.160 7 50959497 intron variant A/C snv 0.96 2
rs3132453
PRRC2A
0.925 0.200 6 31636267 missense variant T/G snv 0.96 0.95 1
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 13
rs3130933
POU5F1 ; TCF19
0.882 0.200 6 31164308 intron variant T/C snv 0.92 2
rs9267658
CYP21A2 ; SLC44A4 ; EHMT2-AS1
0.882 0.240 6 31878208 intron variant T/C snv 0.91 3
rs3132946
NOTCH4
0.882 0.240 6 32222251 intron variant A/G snv 0.91 3
rs3134954
TNXB
0.882 0.240 6 32104116 intron variant C/T snv 0.90 3
rs3130050
APOM ; BAG6
0.882 0.240 6 31650984 intron variant G/A snv 0.89 3
rs9267992 0.882 0.240 6 32252620 upstream gene variant G/A snv 0.89 3
rs2905722
MICB-DT
0.925 0.120 6 31481550 intron variant A/G snv 0.88 5
rs9267649 0.882 0.240 6 31857051 downstream gene variant A/G snv 0.88 3
rs550448
JAZF1-AS1
1.000 0.120 7 28189423 intron variant G/A snv 0.86 1
rs1634731
MUC21
1.000 0.120 6 30987904 intron variant G/A snv 0.86 1
rs10810632
BNC2
1.000 0.120 9 16789026 intron variant C/T snv 0.85 1
rs2254556 0.851 0.280 6 31374854 intron variant T/C snv 0.85 3
rs2542151 0.763 0.480 18 12779948 upstream gene variant G/T snv 0.83 6
rs3129934
TSBP1 ; TSBP1-AS1
0.925 0.160 6 32368410 intron variant T/C snv 0.83 2
rs3130361 0.925 0.160 6 30371787 intergenic variant A/G snv 0.81 3
rs6457374
HLA-B ; LOC112267902
0.851 0.200 6 31304484 intron variant C/T snv 0.81 7
rs566369
LOC107983981
1.000 0.120 15 53216395 intergenic variant A/G snv 0.81 1
rs482541
LOC107983981
1.000 0.120 15 53216997 intergenic variant A/G snv 0.81 1
rs3129888
HLA-DRA
0.882 0.240 6 32443949 intron variant G/A snv 0.82 0.80 3
rs8007115 1.000 0.120 14 94871151 intergenic variant T/C snv 0.80 1
rs2247056
LOC112267902 ; HLA-B ; LINC02571
0.882 0.160 6 31297713 intron variant T/C snv 0.80 8