Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11206510 0.763 0.240 1 55030366 intergenic variant T/A;C;G snv 7
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 6
rs4299376
LOC102725159 ; ABCG8
0.851 0.120 2 43845437 intron variant G/C;T snv 6
rs1333040
CDKN2B-AS1
0.732 0.280 9 22083405 intron variant C/G;T snv 4
rs1805007
MC1R
0.695 0.280 16 89919709 missense variant C/A;G;T snv 4.4E-02 4
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
rs17577
SLC12A5-AS1 ; MMP9
0.649 0.520 20 46014472 missense variant G/A;C snv 0.16 1
rs17879961
CHEK2
0.597 0.480 22 28725099 missense variant A/C;G snv 4.1E-03 1
rs6503659 1.000 0.040 17 41741012 intergenic variant A/C;G;T snv 1
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 10
rs11571833
BRCA2
0.608 0.360 13 32398489 stop gained A/T snv 6.6E-03 6.0E-03 2
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 6
rs4803750
BCL3
0.807 0.240 19 44744370 upstream gene variant A/G snv 7.7E-02 6
rs7412
APOE
0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 5
rs4785204
HEATR3
1.000 0.040 16 50069823 intron variant C/T snv 8.6E-02 1
rs12296850 0.925 0.080 12 100426307 downstream gene variant A/G snv 8.7E-02 1
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
rs72928038
BACH2
0.695 0.360 6 90267049 intron variant G/A snv 0.11 1
rs6511720
LDLR
0.790 0.120 19 11091630 intron variant G/T snv 0.12 10
rs4149056
SLCO1B1
0.633 0.480 12 21178615 missense variant T/C snv 0.13 0.12 5
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 20
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