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
rs855791
TMPRSS6
0.701 0.400 22 37066896 missense variant A/G;T snv 0.57; 4.0E-06 8
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
rs11066188
HECTD4
0.851 0.320 12 112172910 intron variant G/A;C snv 0.30; 4.1E-06 4
rs212388
LOC112267968 ; LOC105378083
0.827 0.240 6 159069404 intron variant C/G;T snv 4
rs763361
CD226
0.689 0.520 18 69864406 missense variant T/A;C snv 4.0E-06; 0.52 4
rs1980422 0.776 0.320 2 203745673 intergenic variant C/A;T snv 3
rs654690
LOC112267968
1.000 0.080 6 159093746 intron variant T/A;C snv 3
rs12734338
PPP1R12B
0.925 0.120 1 202500595 intron variant T/C snv 2
rs17264332 0.925 0.200 6 137684378 intron variant A/G;T snv 2
rs1893592
UBASH3A
0.742 0.280 21 42434957 missense variant A/C;G snv 0.27; 8.0E-06 2
rs2069772
IL2
0.925 0.200 4 122451978 intron variant T/A;C snv 2
rs424232 0.882 0.240 6 32240547 intergenic variant C/A;T snv 2
rs4246905
TNFSF15
0.716 0.400 9 114790969 missense variant T/A;C snv 0.76 2
rs7579944 0.882 0.200 2 30222160 intergenic variant T/C;G snv 2