Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3130564
PSORS1C1
0.790 0.360 6 31133897 intron variant C/T snv 0.14 5
rs3132610
ABCF1
0.807 0.280 6 30576624 intron variant A/G snv 7.4E-02 5
rs3132685
HLA-A ; HCG9
0.807 0.320 6 29978172 intron variant G/A;T snv 5
rs3806156
BTNL2 ; TSBP1-AS1
0.827 0.280 6 32405921 intron variant G/A;T snv 5
rs3817963
TSBP1-AS1 ; BTNL2
0.776 0.360 6 32400310 intron variant T/C snv 0.25 5
rs4386816
HLA-B
0.925 0.120 6 31279358 intron variant T/C snv 0.17 5
rs6903608
HLA-DRB9
0.742 0.400 6 32460508 intron variant C/G;T snv 5
rs7453920
HLA-DQB2
0.752 0.440 6 32762235 intron variant A/G;T snv 5
rs910049
TSBP1-AS1 ; TSBP1
0.776 0.400 6 32347950 intron variant T/C snv 0.76 5
rs9268645
HLA-DRA
0.827 0.360 6 32440750 intron variant C/G;T snv 5
rs10758593
GLIS3
0.827 0.240 9 4292083 intron variant G/A snv 0.45 4
rs12708716
CLEC16A
0.807 0.320 16 11086016 intron variant A/G snv 0.37 4
rs1480380
HLA-DMB
0.763 0.360 6 32945469 intron variant C/T snv 0.11 4
rs204990
GPSM3
0.851 0.280 6 32193653 intron variant C/A;T snv 4
rs2051549
HLA-DQB2
0.851 0.280 6 32762309 intron variant G/A snv 0.64 4
rs2292239
ERBB3
0.742 0.480 12 56088396 intron variant T/G snv 0.65 4
rs3115553
TSBP1-AS1
0.851 0.200 6 32278050 intron variant C/T snv 0.25 4
rs3129791
HCG15
0.827 0.280 6 28986516 intron variant G/A snv 5.3E-02 4
rs3129939
TSBP1-AS1 ; TSBP1
0.827 0.360 6 32368989 intron variant A/G snv 0.14 4
rs3129943
TSBP1-AS1 ; TSBP1
0.851 0.240 6 32370918 intron variant A/G snv 0.26 4
rs3130340
TSBP1-AS1
0.851 0.200 6 32276850 intron variant T/C snv 0.25 4
rs4402960
IGF2BP2
0.724 0.400 3 185793899 intron variant G/T snv 0.38 4
rs4506565
TCF7L2
0.790 0.280 10 112996282 intron variant A/G;T snv 4
rs706778
IL2RA
0.695 0.320 10 6056986 intron variant C/T snv 0.46 4
rs707928
VWA7
0.827 0.320 6 31774813 intron variant A/G snv 0.47 4