Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 6
rs7138803 0.827 0.240 12 49853685 intergenic variant G/A;T snv 6
rs10094715 0.925 0.040 8 46473341 intergenic variant A/G snv 9.8E-03 2
rs1111875 0.776 0.360 10 92703125 intergenic variant C/T snv 0.36 2
rs12314274 0.925 0.040 12 85855418 intergenic variant T/C snv 0.37 2
rs12362105 0.925 0.040 11 76739864 intergenic variant G/A;T snv 2
rs17066440 0.925 0.040 18 59981043 intergenic variant T/C snv 3.3E-02 2
rs2384506 0.851 0.080 12 114991548 intergenic variant T/C snv 0.21 2
rs2865108 0.925 0.040 7 67861752 intergenic variant C/A snv 0.89 2
rs41440452 0.925 0.040 9 122717961 intergenic variant G/A snv 7.9E-02 2
rs6756629
ABCG5 ; ABCG8
0.925 0.080 2 43837951 missense variant G/A;T snv 6.7E-02 4
rs11887534
ABCG5 ; ABCG8
0.653 0.440 2 43839108 missense variant G/A;C snv 6.4E-06; 6.7E-02 2
rs4953023
ABCG8
0.925 0.040 2 43846861 non coding transcript exon variant G/A snv 6.9E-02 5
rs4245791
ABCG8
0.882 0.080 2 43847292 non coding transcript exon variant C/A;T snv 4
rs4148217
ABCG8
0.790 0.280 2 43872294 missense variant C/A;T snv 0.21; 1.2E-05 3
rs41360247
ABCG8 ; LOC102725159
0.882 0.080 2 43846517 non coding transcript exon variant T/C snv 7.9E-02 2
rs693
APOB
0.708 0.440 2 21009323 synonymous variant G/A snv 0.39 0.38 7
rs1011770
BAZ2B
0.925 0.040 2 159382207 intron variant A/G snv 2.5E-02 2
rs135851
C22orf34
0.925 0.040 22 49583909 intron variant A/C snv 4.4E-02 2
rs9906298
CA10
0.925 0.040 17 51702890 intron variant T/C snv 9.2E-02 2
rs708272
CETP
0.708 0.440 16 56962376 intron variant G/A snv 0.42 0.38 4
rs17088392
DACH1
0.925 0.040 13 71683104 intron variant T/C snv 8.5E-02 2
rs41506144
FRMD4A
0.925 0.040 10 13834687 intron variant C/G;T snv 2
rs17063627
GNA14
0.925 0.040 9 77424742 intron variant A/G snv 7.2E-02 2
rs738785
GUSBP11
0.925 0.040 22 23680444 intron variant C/T snv 0.49 2