Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 24
rs1464510
LPP
0.807 0.280 3 188394766 intron variant C/A;T snv 7
rs917997 0.701 0.480 2 102454108 downstream gene variant T/A;C snv 6
rs11221332
ETS1
0.763 0.280 11 128511079 intron variant C/A;T snv 5
rs1250552
ZMIZ1
0.882 0.200 10 79298270 intron variant A/C;G snv 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
rs13314993
LOC105377022
0.882 0.200 3 32973977 regulatory region variant G/C;T snv 5
rs17035378
PLEK ; LOC101927723
0.882 0.200 2 68371823 intron variant T/A;C snv 5
rs4819388
ICOSLG
0.790 0.240 21 44227538 3 prime UTR variant T/C snv 5
rs802734 0.827 0.280 6 127957653 intergenic variant A/G;T snv 5
rs9792269 0.882 0.200 8 128252343 intergenic variant A/C;G snv 5
rs212388
LOC112267968 ; LOC105378083
0.827 0.240 6 159069404 intron variant C/G;T snv 4
rs4750316
LINC02649 ; LINC02656
0.882 0.160 10 6351298 non coding transcript exon variant C/G;T snv 4
rs4810485
CD40
0.732 0.480 20 46119308 intron variant T/A;G snv 4
rs6421571 0.851 0.200 11 118873063 intergenic variant T/A;C snv 3
rs654690
LOC112267968
1.000 0.080 6 159093746 intron variant T/A;C snv 3
rs657555
PTPN2
0.925 0.080 18 12847137 intron variant C/A;T snv 3
rs10932019 2 203764087 downstream gene variant G/A;C snv 2
rs1772408
IFI16
1 159035859 intron variant A/G;T snv 2
rs6848139 1.000 0.040 4 122473886 intergenic variant A/C;G snv 2
rs7523907
LOC101928512 ; CD247
1.000 0.080 1 167458010 non coding transcript exon variant C/A;T snv 2
rs7579944 0.882 0.200 2 30222160 intergenic variant T/C;G snv 2
rs7678445
KIAA1109
4 122361617 intron variant G/A;T snv 2
rs926657
TAGAP ; LOC105378083
6 159042420 non coding transcript exon variant C/G;T snv 2