Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2188962
IRF1-AS1
0.882 0.160 5 132435113 intron variant C/T snv 0.29 4
rs864745
JAZF1
0.763 0.320 7 28140937 intron variant T/C snv 0.41 4
rs3764147
LACC1
0.807 0.280 13 43883789 missense variant A/G snv 0.28 0.27 4
rs1736135
LOC101927745
0.851 0.160 21 15432901 intron variant T/C snv 0.33 4
rs694739
LOC102723878
0.763 0.320 11 64329761 upstream gene variant A/G snv 0.28 4
rs212388
LOC112267968 ; LOC105378083
0.827 0.240 6 159069404 intron variant C/G;T snv 4
rs11584383
MROH3P
0.827 0.200 1 200966738 downstream gene variant T/C snv 0.24 4
rs11190140
NKX2-3 ; LINC01475
0.827 0.160 10 99531836 upstream gene variant T/C snv 0.55 4
rs10045431 0.851 0.240 5 159387525 intron variant A/C snv 0.78 3
rs10865331 0.827 0.120 2 62324337 intergenic variant A/G snv 0.57 3
rs10995271 0.776 0.280 10 62678726 downstream gene variant G/C snv 0.32 3
rs12232497 0.701 0.360 17 39883866 intergenic variant T/C snv 0.35 3
rs13192471 0.925 0.160 6 32703326 downstream gene variant T/C snv 0.19 3
rs1456893 0.851 0.160 7 50230076 intron variant G/A snv 0.69 3
rs17391694 0.882 0.120 1 78157942 regulatory region variant C/T snv 7.8E-02 3
rs17582416 0.882 0.160 10 34998722 regulatory region variant T/G snv 0.31 3
rs2006996 0.882 0.080 9 114830358 regulatory region variant T/C snv 7.2E-02 3
rs2794520 0.807 0.240 1 159709026 upstream gene variant C/A;T snv 3
rs4613763 0.851 0.240 5 40392626 regulatory region variant T/C snv 0.14 3
rs4728142 0.732 0.320 7 128933913 upstream gene variant G/A snv 0.38 3
rs6421571 0.851 0.200 11 118873063 intergenic variant T/A;C snv 3
rs7746082 0.851 0.160 6 105987394 regulatory region variant G/A;C snv 3
rs7765379 0.827 0.280 6 32713151 upstream gene variant T/G snv 0.10 3
rs9275328 0.851 0.240 6 32699045 intergenic variant C/T snv 0.16 3
rs2231142
ABCG2
0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12 3