Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs693
APOB
0.708 0.440 2 21009323 synonymous variant G/A snv 0.39 0.38 7
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
rs4299376
LOC102725159 ; ABCG8
0.851 0.120 2 43845437 intron variant G/C;T snv 6
rs887829
UGT1A8 ; UGT1A5 ; UGT1A6 ; UGT1A7 ; UGT1A4 ; UGT1A3 ; UGT1A10 ; UGT1A1 ; UGT1A9
0.763 0.280 2 233759924 intron variant C/T snv 0.36 6
rs4953023
ABCG8
0.925 0.040 2 43846861 non coding transcript exon variant G/A snv 6.9E-02 5
rs1800961
HNF4A
0.851 0.160 20 44413724 missense variant C/T snv 3.1E-02 2.5E-02 5
rs738409
PNPLA3
0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 5
rs6756629
ABCG5 ; ABCG8
0.925 0.080 2 43837951 missense variant G/A;T snv 6.7E-02 4
rs4245791
ABCG8
0.882 0.080 2 43847292 non coding transcript exon variant C/A;T snv 4
rs708272
CETP
0.708 0.440 16 56962376 intron variant G/A snv 0.42 0.38 4
rs4148217
ABCG8
0.790 0.280 2 43872294 missense variant C/A;T snv 0.21; 1.2E-05 3
rs2072183
NPC1L1
0.925 0.040 7 44539581 synonymous variant G/A;C snv 4.0E-06; 0.25 3
rs4148323
UGT1A10 ; UGT1A9 ; UGT1A7 ; UGT1A3 ; UGT1A5 ; UGT1A6 ; UGT1A8 ; UGT1A1 ; UGT1A4
0.701 0.440 2 233760498 missense variant G/A snv 2.2E-02 9.2E-03 3
rs6742078
UGT1A3 ; UGT1A7 ; UGT1A8 ; UGT1A10 ; UGT1A6 ; UGT1A4 ; UGT1A9 ; UGT1A1 ; UGT1A5
0.807 0.240 2 233763993 intron variant G/T snv 0.36 3
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
rs11887534
ABCG5 ; ABCG8
0.653 0.440 2 43839108 missense variant G/A;C snv 6.4E-06; 6.7E-02 2
rs41360247
ABCG8 ; LOC102725159
0.882 0.080 2 43846517 non coding transcript exon variant T/C snv 7.9E-02 2