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
rs11186149
SH2D4B
0.925 0.040 10 80580951 intron variant T/C snv 8.6E-02 2
rs12314274 0.925 0.040 12 85855418 intergenic variant T/C snv 0.37 2
rs16843641
TANC1
0.925 0.040 2 159061866 intron variant T/C snv 1.2E-02 2
rs17066440 0.925 0.040 18 59981043 intergenic variant T/C snv 3.3E-02 2
rs17088392
DACH1
0.925 0.040 13 71683104 intron variant T/C snv 8.5E-02 2
rs2384506 0.851 0.080 12 114991548 intergenic variant T/C snv 0.21 2
rs41360247
ABCG8 ; LOC102725159
0.882 0.080 2 43846517 non coding transcript exon variant T/C snv 7.9E-02 2
rs6598902
STX12
0.925 0.040 1 27779198 intron variant T/C snv 0.18 2
rs9906298
CA10
0.925 0.040 17 51702890 intron variant T/C snv 9.2E-02 2
rs6742078
UGT1A3 ; UGT1A7 ; UGT1A8 ; UGT1A10 ; UGT1A6 ; UGT1A4 ; UGT1A9 ; UGT1A1 ; UGT1A5
0.807 0.240 2 233763993 intron variant G/T snv 0.36 3
rs4299376
LOC102725159 ; ABCG8
0.851 0.120 2 43845437 intron variant G/C;T snv 6
rs7138803 0.827 0.240 12 49853685 intergenic variant G/A;T snv 6
rs6756629
ABCG5 ; ABCG8
0.925 0.080 2 43837951 missense variant G/A;T snv 6.7E-02 4
rs12362105 0.925 0.040 11 76739864 intergenic variant G/A;T snv 2
rs2072183
NPC1L1
0.925 0.040 7 44539581 synonymous variant G/A;C snv 4.0E-06; 0.25 3
rs11887534
ABCG5 ; ABCG8
0.653 0.440 2 43839108 missense variant G/A;C snv 6.4E-06; 6.7E-02 2
rs693
APOB
0.708 0.440 2 21009323 synonymous variant G/A snv 0.39 0.38 7
rs4953023
ABCG8
0.925 0.040 2 43846861 non coding transcript exon variant G/A snv 6.9E-02 5
rs708272
CETP
0.708 0.440 16 56962376 intron variant G/A snv 0.42 0.38 4
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
rs17241442
TNC ; DELEC1
0.925 0.040 9 115062806 intron variant G/A snv 0.11 2
rs2241423
MAP2K5
0.882 0.120 15 67794500 intron variant G/A snv 0.29 2
rs41440452 0.925 0.040 9 122717961 intergenic variant G/A snv 7.9E-02 2
rs8061765
TMEM114
0.925 0.040 16 8540871 intron variant G/A snv 0.11 2