Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7412
APOE
0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 20
rs186696265 0.882 0.040 6 160690668 intergenic variant C/T snv 1.0E-02 6
rs140570886
LPA
1.000 0.040 6 160591981 intron variant T/C snv 2.8E-02 3
rs118039278
LPA
6 160564494 intron variant G/A snv 4.3E-02 2
rs147555597
LPAL2
1.000 0.040 6 160490564 intron variant G/A snv 5.5E-03 2
rs41269133 1.000 0.040 6 160666831 intron variant T/C snv 8.8E-02 2
rs41272114
LPA
1.000 0.040 6 160585045 splice donor variant C/A;T snv 1.2E-05; 4.1E-02 2
rs4252185
PLG
1.000 0.040 6 160702419 intron variant T/C snv 5.7E-02 2
rs55730499
LPA
1.000 0.040 6 160584578 intron variant C/T snv 4.5E-02 2
rs6926458
LPA
1.000 0.040 6 160598834 intron variant A/G;T snv 2
rs73596816
LPA
1.000 0.040 6 160596331 intron variant G/A snv 3.6E-02 2
rs7770628
LPA
1.000 0.040 6 160597142 intron variant C/T snv 0.63 2
rs1018234
SLC22A3
6 160375026 intron variant C/T snv 0.32 1
rs112842440
LPA
6 160534681 intron variant G/C;T snv 1
rs115848955
LPA
6 160610628 intron variant C/A;T snv 1
rs116850263
LPA
6 160608638 intron variant T/A;C snv 1
rs117026595
LPA
6 160647203 intron variant A/T snv 8.9E-03 1
rs12204009
SLC22A3
6 160378214 intron variant T/C snv 2.8E-03 1
rs12207325
LPAL2
6 160482879 intron variant G/A snv 7.1E-03 1
rs12529361
PLG
6 160704599 intron variant T/C snv 0.18 1
rs12664092 6 160527104 downstream gene variant A/C;G snv 1
rs12787909
DSCAML1
11 117675767 intron variant A/G snv 3.6E-02 1
rs1367211
LPA
6 160661663 intron variant T/C snv 0.66 1
rs139699952
LOC105378091
6 160800348 intergenic variant G/C snv 2.6E-02 1
rs1406888 6 160670561 intron variant C/T snv 0.46 1