Disease: Serum LDL cholesterol measurement
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
rs11591147
PCSK9
0.677 0.360 1 55039974 missense variant G/A;T snv 1.2E-02 4
rs12740374
CELSR2
0.851 0.040 1 109274968 3 prime UTR variant G/T snv 0.22 8
rs4844614
CR1L
1.000 0.040 1 207701830 intron variant G/C;T snv 3
rs599839
PSRC1
0.724 0.360 1 109279544 downstream gene variant G/A;C snv 9
rs629301
CELSR2
0.851 0.120 1 109275684 3 prime UTR variant G/T snv 0.74 8
rs646776
CELSR2
0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 10
rs515135 0.807 0.160 2 21063185 intergenic variant T/C snv 0.73 6
rs562338 0.807 0.160 2 21065449 intergenic variant A/G snv 0.69 6
rs6544713
ABCG8
0.925 0.040 2 43846742 non coding transcript exon variant T/C snv 0.75 5
rs6756629
ABCG5 ; ABCG8
0.925 0.080 2 43837951 missense variant G/A;T snv 6.7E-02 4
rs693
APOB
0.708 0.440 2 21009323 synonymous variant G/A snv 0.39 0.38 7
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 24
rs12654264
HMGCR
0.925 0.120 5 75352778 intron variant A/T snv 0.38 5
rs1501908 1.000 0.040 5 156971158 intergenic variant G/A;C;T snv 3
rs3846662
HMGCR
0.763 0.280 5 75355259 non coding transcript exon variant A/G snv 0.50 0.58 5
rs3846663
HMGCR ; CERT1
0.882 0.120 5 75359901 intron variant C/T snv 0.35 4
rs7703051 0.851 0.120 5 75329662 intron variant C/A snv 0.38 3
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 6
rs2254287
COL11A2
1.000 0.040 6 33176171 intron variant C/A;G;T snv 3
rs3798220
LPA
0.732 0.160 6 160540105 missense variant T/C snv 5.6E-02 3.1E-02 4
rs12670798
DNAH11 ; LOC105375183
1.000 0.040 7 21567734 intron variant T/C snv 0.26 4
rs17321515 0.776 0.200 8 125474167 intron variant A/G snv 0.49 7
rs579459 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 17
rs174546
FADS1 ; FADS2
0.807 0.200 11 61802358 3 prime UTR variant C/T snv 0.28 9