Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6942328
LOC105374894
6 4512745 intron variant T/C snv 3.3E-03 1
rs7209801 17 44246008 downstream gene variant G/A snv 0.38 1
rs7232775
SLC14A2
18 45622439 intron variant C/T snv 0.76 1
rs877282 10 725592 intergenic variant G/A snv 0.13 1
rs12801636
PCNX3
1.000 0.040 11 65623846 intron variant G/A snv 0.25 2
rs13226650
MLXIPL
1.000 0.040 7 73602675 intron variant A/G snv 0.19 2
rs889472
LOC101928230
0.925 0.040 16 79612092 intergenic variant C/A;G snv 1
rs9271585 1.000 0.040 6 32623102 regulatory region variant C/A snv 0.27 1
rs174455
FADS3
1.000 0.080 11 61888645 intron variant G/A;C snv 3
rs11066453
OAS1
1.000 0.080 12 112927816 intron variant A/G snv 3.8E-03 2
rs11949767
MXD3
1.000 0.080 5 177313243 upstream gene variant A/C;G snv 2
rs3925584
LOC101928338
1.000 0.080 11 30738788 intergenic variant T/C snv 0.35 2
rs10109414 1.000 0.080 8 23893638 regulatory region variant C/T snv 0.37 1
rs1800574
HNF1A ; HNF1A-AS1
0.882 0.080 12 120979061 missense variant C/T snv 2.9E-02 2.2E-02 1
rs626277
DACH1
1.000 0.080 13 71773564 intron variant A/C snv 0.51 1
rs17145750
MLXIPL
0.925 0.120 7 73612048 intron variant C/A;T snv 7
rs1051921
MLXIPL
0.925 0.120 7 73593613 3 prime UTR variant G/A snv 0.15 6
rs3823418
PSORS1C1
0.925 0.120 6 31133165 intron variant G/A snv 0.23 6
rs1150660 0.925 0.120 6 26101212 upstream gene variant A/C snv 0.73 5
rs115810
TRIM38
0.925 0.120 6 25975655 intron variant G/A;C snv 5
rs1178977
BAZ1B
0.925 0.120 7 73442719 splice region variant A/G snv 0.16 0.21 5
rs129129
TRIM38
0.925 0.120 6 25960801 upstream gene variant A/G snv 0.73 5
rs1540276
H4C2
0.925 0.120 6 26028591 upstream gene variant T/A;G snv 5
rs198853
H4C3
0.925 0.120 6 26103868 upstream gene variant T/C snv 0.28 5
rs199726 0.925 0.120 6 25953132 intergenic variant G/A snv 0.73 5