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
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
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
rs4245791
ABCG8
0.882 0.080 2 43847292 non coding transcript exon variant C/A;T snv 4
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
rs1011770
BAZ2B
0.925 0.040 2 159382207 intron variant A/G snv 2.5E-02 2
rs10888095
SGCZ
0.925 0.040 8 15004905 intron variant C/A;G snv 2
rs10998022
MYPN
0.925 0.040 10 68210229 intron variant C/T snv 0.26 2
rs1111875 0.776 0.360 10 92703125 intergenic variant C/T snv 0.36 2
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
rs12362105 0.925 0.040 11 76739864 intergenic variant G/A;T snv 2
rs135851
C22orf34
0.925 0.040 22 49583909 intron variant A/C snv 4.4E-02 2
rs1475029
LOC729296 ; MIR646HG
0.925 0.040 20 60093953 intron variant A/G snv 0.23 2
rs16824658
HMCN1
0.925 0.040 1 185895380 intron variant A/G snv 7.6E-02 2
rs16843641
TANC1
0.925 0.040 2 159061866 intron variant T/C snv 1.2E-02 2
rs17063627
GNA14
0.925 0.040 9 77424742 intron variant A/G snv 7.2E-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
rs17241442
TNC ; DELEC1
0.925 0.040 9 115062806 intron variant G/A snv 0.11 2
rs2013647
ZNF28
0.925 0.040 19 52827416 intron variant C/T snv 0.11 2
rs2241423
MAP2K5
0.882 0.120 15 67794500 intron variant G/A snv 0.29 2