Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs8187710
ABCC2
0.827 0.200 10 99851537 missense variant G/A snv 5.3E-02 8.5E-02 6
rs7660895
SLC2A9
0.882 0.200 4 9983821 intron variant A/G;T snv 5
rs2740574
CYP3A4
0.807 0.360 7 99784473 upstream gene variant C/T snv 0.78 12
rs55951658
CYP3A4
0.827 0.200 7 99770202 missense variant T/A;C snv 4.1E-04 9.8E-05 7
rs4646437
CYP3A4
0.827 0.200 7 99767460 intron variant G/A snv 0.30 8
rs2242480
CYP3A4
0.882 0.120 7 99763843 intron variant C/T snv 0.22 0.32 5
rs669676
COL8A1
1.000 0.040 3 99730008 intron variant A/G snv 0.45 2
rs13095226
COL8A1
0.851 0.040 3 99677428 intron variant T/C snv 9.5E-02 5
rs776746
CYP3A5 ; ZSCAN25
0.724 0.400 7 99672916 splice acceptor variant T/C snv 0.72 21
rs4905794
LOC107984696
1.000 0.040 14 99013332 intergenic variant G/A;C;T snv 2
rs2654981
IGF1R
15 98961900 3 prime UTR variant C/G;T snv 1
rs1815009
IGF1R
0.925 0.080 15 98961442 3 prime UTR variant C/T snv 0.65 3
rs2002880
IGF1R
1.000 0.080 15 98960516 3 prime UTR variant G/A snv 3.6E-03 2
rs2229765
IGF1R
0.807 0.280 15 98934996 synonymous variant G/A snv 0.40 0.39 7
rs2684761
IGF1R
15 98821141 intron variant A/G snv 0.47 1
rs187821766
STK3
8 98729050 intron variant C/T snv 3.5E-03 3
rs13379905
IRAIN ; IGF1R
1.000 0.040 15 98649254 5 prime UTR variant C/A;T snv 2
rs186208701
STK3
8 98567888 intron variant T/C snv 3.3E-03 3
rs653747
LINC00923
15 97659878 intron variant C/T snv 0.48 2
rs4910498
SWAP70
11 9743956 intron variant A/T snv 0.61 4
rs2649044
SWAP70
11 9742422 intron variant C/T snv 0.55 4
rs4857055
EPHA6
3 97192120 intron variant C/T snv 5.0E-02 2
rs2927615
ERAP1
5 96862499 intron variant G/A snv 0.18 1
rs30187
ERAP1
0.732 0.360 5 96788627 missense variant T/A;C snv 0.62 14
rs10050860
ERAP1
0.882 0.240 5 96786506 missense variant C/T snv 0.15 0.16 4