Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4149056
SLCO1B1
0.633 0.480 12 21178615 missense variant T/C snv 0.13 0.12 45
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 22
rs2306283
SLCO1B1
0.742 0.320 12 21176804 missense variant A/G;T snv 0.47 16
rs774010631
UGT1A8 ; UGT1A7 ; UGT1A6 ; UGT1A4 ; UGT1A9 ; UGT1A10 ; UGT1A5
0.827 0.160 2 233719115 missense variant G/C snv 2.4E-05 2.1E-05 5
rs11045819
SLCO1B1
0.851 0.120 12 21176879 missense variant C/A;T snv 0.11; 4.0E-06 4
rs72554664
G6PD
0.882 0.160 X 154532257 missense variant C/T snv 5.5E-04 1.1E-04 3
rs33947415
HBB
0.882 0.120 11 5226684 missense variant C/G;T snv 9.4E-04 3
rs10929303
MROH2A ; UGT1A5 ; UGT1A9 ; UGT1A8 ; UGT1A1 ; UGT1A10 ; UGT1A3 ; UGT1A7 ; UGT1A4 ; UGT1A6
1.000 0.080 2 233772770 3 prime UTR variant T/C snv 0.74 3
rs368362776
UGT1A10 ; UGT1A9 ; UGT1A6 ; UGT1A7 ; UGT1A8
0.882 0.120 2 233693633 missense variant C/G;T snv 4.0E-06 3
rs1042640
UGT1A4 ; MROH2A ; UGT1A6 ; UGT1A7 ; UGT1A3 ; UGT1A5 ; UGT1A9 ; UGT1A8 ; UGT1A1 ; UGT1A10
1.000 0.080 2 233772898 3 prime UTR variant G/A;C;T snv 3
rs113683735
HMOX1
0.925 0.080 22 35386751 missense variant A/G snv 2
rs699512
LOC102724946 ; BLVRA
0.925 0.120 7 43771165 missense variant G/A snv 0.80 0.83 2
rs10157822 1.000 0.080 1 161242119 upstream gene variant T/C snv 0.40 1
rs2307424
NR1I3
1.000 0.080 1 161232815 synonymous variant G/A snv 0.35 0.29 1
rs4073054
TOMM40L ; NR1I3
1.000 0.080 1 161230697 3 prime UTR variant C/A;G;T snv 1