Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs4245791
ABCG8
0.882 0.080 2 43847292 non coding transcript exon variant C/A;T snv 4
rs6756629
ABCG5 ; ABCG8
0.925 0.080 2 43837951 missense variant G/A;T snv 6.7E-02 4
rs2072183
NPC1L1
0.925 0.040 7 44539581 synonymous variant G/A;C snv 4.0E-06; 0.25 3
rs4148217
ABCG8
0.790 0.280 2 43872294 missense variant C/A;T snv 0.21; 1.2E-05 3
rs10888095
SGCZ
0.925 0.040 8 15004905 intron variant C/A;G snv 2
rs11887534
ABCG5 ; ABCG8
0.653 0.440 2 43839108 missense variant G/A;C snv 6.4E-06; 6.7E-02 2
rs12362105 0.925 0.040 11 76739864 intergenic variant G/A;T snv 2
rs41506144
FRMD4A
0.925 0.040 10 13834687 intron variant C/G;T snv 2
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
rs10094715 0.925 0.040 8 46473341 intergenic variant A/G snv 9.8E-03 2
rs16843641
TANC1
0.925 0.040 2 159061866 intron variant T/C snv 1.2E-02 2
rs1800961
HNF4A
0.851 0.160 20 44413724 missense variant C/T snv 3.1E-02 2.5E-02 5
rs1011770
BAZ2B
0.925 0.040 2 159382207 intron variant A/G snv 2.5E-02 2
rs17066440 0.925 0.040 18 59981043 intergenic variant T/C snv 3.3E-02 2
rs135851
C22orf34
0.925 0.040 22 49583909 intron variant A/C snv 4.4E-02 2
rs8083296
L3MBTL4
0.925 0.040 18 6158717 intron variant A/C snv 5.4E-02 2
rs4953023
ABCG8
0.925 0.040 2 43846861 non coding transcript exon variant G/A snv 6.9E-02 5
rs253314
MYO10
0.925 0.040 5 16871155 intron variant A/C snv 6.9E-02 2
rs17063627
GNA14
0.925 0.040 9 77424742 intron variant A/G snv 7.2E-02 2
rs16824658
HMCN1
0.925 0.040 1 185895380 intron variant A/G snv 7.6E-02 2
rs41360247
ABCG8 ; LOC102725159
0.882 0.080 2 43846517 non coding transcript exon variant T/C snv 7.9E-02 2
rs41440452 0.925 0.040 9 122717961 intergenic variant G/A snv 7.9E-02 2
rs17088392
DACH1
0.925 0.040 13 71683104 intron variant T/C snv 8.5E-02 2