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
rs11206510 0.763 0.240 1 55030366 intergenic variant T/A;C;G snv 7
rs4299376
LOC102725159 ; ABCG8
0.851 0.120 2 43845437 intron variant G/C;T snv 6
rs2239612
ST6GAL1
1.000 0.040 3 187075454 intron variant G/A snv 0.17 1
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 6
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
rs3846662
HMGCR
0.763 0.280 5 75355259 non coding transcript exon variant A/G snv 0.50 0.58 5
rs2853676
TERT
0.667 0.560 5 1288432 intron variant T/A;C snv 4
rs16891982
SLC45A2
0.776 0.200 5 33951588 missense variant C/A;G snv 0.65 3
rs2736098
TERT
0.600 0.600 5 1293971 synonymous variant C/T snv 0.29 0.22 1
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 6
rs12203592
IRF4
0.649 0.320 6 396321 intron variant C/T snv 0.10 5
rs12210050
LOC105374875
0.807 0.040 6 475489 non coding transcript exon variant C/T snv 0.11 1
rs1800625
AGER ; PBX2
0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15 1
rs2494938
LRFN2
0.752 0.240 6 40568389 intron variant G/A snv 0.51 1
rs72928038
BACH2
0.695 0.360 6 90267049 intron variant G/A snv 0.11 1
rs2285947
DNAH11
0.807 0.120 7 21544470 intron variant G/A snv 0.44 1
rs987525
CCDC26
0.807 0.160 8 128933908 intron variant C/A snv 0.31 1
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
rs2274223
PLCE1
0.620 0.400 10 94306584 missense variant A/G snv 0.28 0.31 3
rs1042602
LOC107984363 ; TYR
0.925 0.080 11 89178528 missense variant C/A snv 0.25 0.24 2
rs1126809
LOC107984363 ; TYR
0.683 0.320 11 89284793 missense variant G/A snv 0.18 0.18 1
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 10