Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4986910
CYP3A4
0.925 0.080 7 99760901 missense variant A/G snv 5.2E-03 5.1E-03 3
rs1801265
DPYD
0.763 0.280 1 97883329 missense variant A/G snv 0.28 13
rs768288280
DPYD
1.000 0.080 1 97740403 missense variant T/C snv 4.0E-06 2
rs2297595
DPYD
0.776 0.320 1 97699535 missense variant T/C snv 8.5E-02 8.1E-02 10
rs397518423
PIK3CD
0.790 0.240 1 9726972 missense variant G/A snv 10
rs67376798
DPYD
0.851 0.120 1 97082391 missense variant T/A snv 2.8E-03 3.3E-03 9
rs2274407
ABCC4
0.882 0.120 13 95206781 missense variant C/A;G;T snv 9.7E-02 0.10 4
rs766715154
ABCC4
13 95206759 missense variant T/C;G snv 4.0E-06 1
rs218916 1.000 0.040 8 89688709 intron variant C/T snv 0.67 2
rs160441 1.000 0.040 8 89644760 intron variant T/C snv 0.55 2
rs2231142
ABCG2
0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12 56
rs190521996
PMM2
0.790 0.320 16 8811660 missense variant T/C snv 2.9E-04 4.1E-04 12
rs80338701
PMM2
0.776 0.360 16 8811088 stop gained C/A;T snv 4.4E-05; 5.4E-06 14
rs2290280
CCNH ; LOC105379066
5 87412904 5 prime UTR variant C/A;T snv 1
rs7694379 1.000 4 87265357 intron variant G/A snv 0.40 3
rs1441937959
EFL1
0.763 0.280 15 82240555 missense variant T/C snv 8.2E-06 20
rs9574547 13 80057282 intron variant C/A snv 0.17 1
rs1554162524
ELOVL4
0.882 0.160 6 79925034 splice acceptor variant T/C snv 4
rs4969170
LOC101928674
0.752 0.440 17 78364457 intron variant A/C;G snv 0.54 11
rs735239
CD209
0.851 0.240 19 7748382 upstream gene variant A/G snv 0.26 5
rs2287886
CD209
0.776 0.280 19 7747650 upstream gene variant A/G;T snv 0.66 9
rs4694362
DCK
4 71028147 intron variant C/T snv 0.49 1
rs1695
GSTP1
0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs779449782
VWF
12 6057915 missense variant G/A;C snv 1.6E-05 1.4E-05 1
rs61749384
VWF
0.882 0.080 12 6019502 missense variant G/A snv 5