Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1464510
LPP
0.807 0.280 3 188394766 intron variant C/A;T snv 7
rs2872507 0.752 0.360 17 39884510 intergenic variant G/A;T snv 7
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 6
rs917997 0.701 0.480 2 102454108 downstream gene variant T/A;C snv 6
rs10758669 0.763 0.280 9 4981602 upstream gene variant C/A;T snv 5
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
rs1801274
FCGR2A
0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 5
rs2228145
IL6R
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 5
rs3129890 0.827 0.280 6 32446496 downstream gene variant T/A;C snv 5
rs4129267
IL6R
0.807 0.200 1 154453788 intron variant C/G;T 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
rs6010620
RTEL1 ; RTEL1-TNFRSF6B
0.701 0.360 20 63678486 intron variant A/C;G snv 4
rs1008723
GSDMB
0.925 0.160 17 39910014 intron variant G/C;T snv 3
rs12936231
ZPBP2
0.925 0.160 17 39872867 intron variant C/G;T snv 3
rs3763309
TSBP1-AS1 ; BTNL2
0.882 0.160 6 32408196 upstream gene variant C/A;T snv 3
rs4794820
LRRC3C
0.790 0.160 17 39933091 intron variant A/G;T snv 3
rs4795405
LRRC3C
0.851 0.160 17 39932164 intron variant T/A;C snv 3
rs762421
GATD3A
0.851 0.360 21 44195678 intron variant G/A snv 3