Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs149091175
CYP3A43
0.925 0.080 7 99863601 stop gained C/T snv 3.2E-05 4.2E-05 2
rs680055
CYP3A43
0.851 0.120 7 99859982 missense variant C/A;G snv 6.5E-02 0.13 5
rs800672
CYP3A43
0.925 0.080 7 99838575 intron variant G/A snv 0.58 2
rs2740574
CYP3A4
0.807 0.360 7 99784473 upstream gene variant C/T snv 0.78 12
rs11902236
GRHL1
0.925 0.080 2 9977740 intron variant C/T snv 0.36 2
rs775220785
CYP3A4
0.925 0.080 7 99772615 missense variant C/T snv 8.0E-06 4
rs776746
CYP3A5 ; ZSCAN25
0.724 0.400 7 99672916 splice acceptor variant T/C snv 0.72 21
rs1815009
IGF1R
0.925 0.080 15 98961442 3 prime UTR variant C/T snv 0.65 3
rs2684788
IGF1R
0.925 0.080 15 98961208 3 prime UTR variant C/T snv 0.51 2
rs12618769
MGAT4A
0.882 0.120 2 98623468 3 prime UTR variant C/T snv 0.18 3
rs2405942
SHROOM2
0.925 0.080 X 9846095 intron variant G/A snv 2
rs6465657
LMTK2
0.807 0.280 7 98187015 intron variant C/T snv 0.41 0.37 7
rs1052133
OGG1 ; CAMK1
0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs1424375643
OGG1
0.925 0.080 3 9751856 missense variant A/G snv 4.0E-06 2
rs125701
OGG1
0.790 0.160 3 9748794 upstream gene variant G/A snv 0.13 7
rs75718479
RMST
1.000 0.080 12 97483128 intron variant C/A snv 7.4E-02 1
rs750392184
PIK3CD
0.882 0.160 1 9724850 missense variant G/A snv 4.0E-06 3
rs2066479
HSD17B3
0.790 0.160 9 96235528 missense variant C/A;G;T snv 7.2E-02 7
rs1978331
LTA4H
0.827 0.200 12 96015423 intron variant A/G snv 0.50 5
rs854560
PON1
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs72552787
PON1
0.925 0.080 7 95315388 missense variant T/C snv 2
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs1434536
BMPR1B
0.925 0.080 4 95154814 3 prime UTR variant C/T snv 0.45 2
rs3742330
DICER1
0.662 0.640 14 95087025 3 prime UTR variant A/G snv 8.7E-02 24
rs17021918
PDLIM5
0.776 0.240 4 94641726 intron variant C/T snv 0.30 8