Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1329568 0.882 0.120 9 37037979 upstream gene variant T/A;G snv 1
rs2741012 1.000 2 233600317 upstream gene variant C/T snv 0.24 1
rs2442719
HLA-B
0.882 0.120 6 31352761 intron variant C/T snv 0.53 1
rs10173355
UGT1A9 ; UGT1A7 ; UGT1A10 ; UGT1A8
1.000 2 233688675 intron variant A/G;T snv 1
rs7691759 0.882 0.120 4 9686390 intron variant T/A;C snv 2
rs4663969
UGT1A6 ; UGT1A9 ; UGT1A3 ; UGT1A10 ; UGT1A5 ; UGT1A4 ; UGT1A8 ; UGT1A7
1.000 2 233746667 intron variant C/A;T snv 2
rs2814778
CADM3-AS1 ; ACKR1
0.763 0.360 1 159204893 5 prime UTR variant T/C snv 0.25 3
rs929596
UGT1A5 ; UGT1A4 ; UGT1A9 ; UGT1A10 ; UGT1A8 ; UGT1A7 ; UGT1A6 ; UGT1A3 ; UGT1A1
0.925 0.040 2 233765830 intron variant A/G snv 0.32 3
rs3755319
UGT1A8 ; UGT1A1 ; UGT1A3 ; UGT1A4 ; UGT1A7 ; UGT1A10 ; UGT1A9 ; UGT1A5 ; UGT1A6
0.925 0.120 2 233758936 intron variant A/C;G;T snv 3
rs4148325
UGT1A8 ; UGT1A5 ; UGT1A10 ; UGT1A7 ; UGT1A1 ; UGT1A9 ; UGT1A3 ; UGT1A4 ; UGT1A6
0.851 0.080 2 233764663 intron variant C/T snv 0.36 3
rs1875263
UGT1A9 ; UGT1A5 ; UGT1A10 ; UGT1A7 ; UGT1A6 ; UGT1A8 ; UGT1A4
1.000 2 233716976 intron variant C/G;T snv 3
rs17863787
UGT1A9 ; UGT1A8 ; UGT1A6 ; UGT1A7 ; UGT1A10
0.925 0.040 2 233702448 intron variant T/G snv 0.30 3
rs111182473 1.000 6 31385912 upstream gene variant G/A;T snv 4
rs11753208 1.000 6 31037655 downstream gene variant C/T snv 9.7E-02 4
rs12185555 1.000 2 226694601 regulatory region variant A/G snv 0.25 4
rs13198903 1.000 6 31376380 upstream gene variant C/T snv 6.3E-02 4
rs13202464 0.925 0.040 6 31376806 upstream gene variant A/G snv 6.3E-02 4
rs16948255 1.000 16 74847922 downstream gene variant C/T snv 3.9E-02 4
rs17207190 1.000 6 31601743 intergenic variant G/A;T snv 2.8E-02 4
rs17324272 1.000 X 133003128 intergenic variant T/C snv 3.2E-03 4
rs2394894 1.000 6 31239143 intergenic variant T/C snv 0.21 4
rs2394895 1.000 6 31239202 intergenic variant T/C snv 0.21 4
rs2394944 1.000 6 31252673 regulatory region variant C/T snv 0.21 4
rs2507976 1.000 6 31384110 upstream gene variant C/A;T snv 4
rs2515919 1.000 6 31596390 upstream gene variant A/G snv 0.31 4