Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67 17
rs17696736
NAA25
0.827 0.240 12 112049014 intron variant A/G snv 0.30 11
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 10
rs1893217
PTPN2
0.742 0.440 18 12809341 intron variant A/G snv 0.12 8
rs4977574
CDKN2B-AS1
0.695 0.520 9 22098575 intron variant A/G;T snv 8
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 8
rs9268853
HLA-DRB9
0.790 0.440 6 32461866 intron variant T/C snv 0.29 8
rs13003464
PUS10
0.827 0.200 2 60959694 intron variant A/G snv 0.50 7
rs1464510
LPP
0.807 0.280 3 188394766 intron variant C/A;T snv 7
rs2523535 0.851 0.200 6 31368473 intron variant A/G snv 0.32 7
rs17810546
IL12A-AS1
0.827 0.440 3 159947262 intron variant A/G snv 8.2E-02 6
rs2290400
GSDMB
0.790 0.360 17 39909987 intron variant T/C snv 0.48 6
rs6920220 0.742 0.440 6 137685367 intron variant G/A snv 0.16 6
rs9264942
LOC112267902 ; HLA-B
0.763 0.400 6 31306603 intron variant T/C snv 0.34 6
rs9272346
HLA-DQA1
0.790 0.320 6 32636595 intron variant G/A snv 0.54 6
rs9391858
TSBP1-AS1 ; TSBP1
0.925 0.080 6 32373621 intron variant A/G snv 0.13 6
rs10806425
BACH2
0.851 0.280 6 90216893 intron variant C/A snv 0.33 5
rs11221332
ETS1
0.763 0.280 11 128511079 intron variant C/A;T snv 5
rs11712165
ARHGAP31
0.882 0.200 3 119399949 intron variant T/G snv 0.30 5
rs1250552
ZMIZ1
0.882 0.200 10 79298270 intron variant A/C;G snv 5
rs12928822
LOC105371082 ; RMI2
0.882 0.200 16 11310036 intron variant C/T snv 0.13 5
rs13010713
LINC01934
0.882 0.200 2 181131318 intron variant A/C;G snv 5
rs13098911
CCR3
0.882 0.200 3 46193709 intron variant C/G;T snv 5
rs13151961
KIAA1109
0.827 0.200 4 122194347 intron variant A/G snv 0.11 5
rs17035378
PLEK ; LOC101927723
0.882 0.200 2 68371823 intron variant T/A;C snv 5