Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs646776
CELSR2
0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 10
rs6511720
LDLR
0.790 0.120 19 11091630 intron variant G/T snv 0.12 10
rs2736100
TERT
0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 9
rs401681
CLPTM1L
0.620 0.640 5 1321972 intron variant C/T snv 0.48 9
rs405509
APOE
0.667 0.480 19 44905579 upstream gene variant T/G snv 0.58 8
rs11206510 0.763 0.240 1 55030366 intergenic variant T/A;C;G snv 7
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 6
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