Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4299376
LOC102725159 ; ABCG8
0.851 0.120 2 43845437 intron variant G/C;T snv 6
rs4803750
BCL3
0.807 0.240 19 44744370 upstream gene variant A/G snv 7.7E-02 6
rs8067378 0.752 0.240 17 39895095 regulatory region variant A/G snv 0.50 6
rs12203592
IRF4
0.649 0.320 6 396321 intron variant C/T snv 0.10 5
rs4977756
CDKN2B-AS1
0.683 0.440 9 22068653 intron variant G/A snv 0.64 5
rs1333040
CDKN2B-AS1
0.732 0.280 9 22083405 intron variant C/G;T snv 4
rs2853676
TERT
0.667 0.560 5 1288432 intron variant T/A;C snv 4
rs2847281
PTPN2
1.000 0.040 18 12821594 intron variant A/G snv 0.32 2
rs12210050
LOC105374875
0.807 0.040 6 475489 non coding transcript exon variant C/T snv 0.11 1
rs12296850 0.925 0.080 12 100426307 downstream gene variant A/G snv 8.7E-02 1
rs17761864
SMG6
1.000 0.040 17 2268343 intron variant C/A snv 0.28 1
rs1800625
AGER ; PBX2
0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15 1
rs2239612
ST6GAL1
1.000 0.040 3 187075454 intron variant G/A snv 0.17 1
rs2239815
XBP1
0.925 0.080 22 28796682 non coding transcript exon variant T/C snv 0.44 1
rs2285947
DNAH11
0.807 0.120 7 21544470 intron variant G/A snv 0.44 1
rs2494938
LRFN2
0.752 0.240 6 40568389 intron variant G/A snv 0.51 1
rs4785204
HEATR3
1.000 0.040 16 50069823 intron variant C/T snv 8.6E-02 1
rs4822983
CHEK2
0.925 0.080 22 28719078 intron variant C/T snv 0.33 1
rs6503659 1.000 0.040 17 41741012 intergenic variant A/C;G;T snv 1
rs7242481
ELP2 ; SLC39A6
0.925 0.080 18 36129254 5 prime UTR variant G/A snv 0.35 1
rs72928038
BACH2
0.695 0.360 6 90267049 intron variant G/A snv 0.11 1
rs7335046 0.807 0.040 13 99389484 downstream gene variant G/C snv 0.80 1
rs987525
CCDC26
0.807 0.160 8 128933908 intron variant C/A snv 0.31 1