Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2622621
ABCG2
0.851 0.240 4 88109768 intron variant C/A;G snv 6
rs4766566
CUX2
0.851 0.200 12 111269073 intron variant C/T snv 0.42 6
rs729761
LOC105375069 ; LOC107986598
0.925 0.120 6 43836834 intron variant T/A;G snv 6
rs10994856
A1CF
0.925 0.120 10 50885488 intron variant G/A snv 0.19 5
rs11066015
ACAD10
0.925 0.120 12 111730205 intron variant G/A snv 5.9E-03 5
rs11072567
NRG4
15 76006403 intron variant A/G snv 0.43 5
rs115810
TRIM38
0.925 0.120 6 25975655 intron variant G/A;C snv 5
rs12801636
PCNX3
1.000 0.040 11 65623846 intron variant G/A snv 0.25 5
rs12908437
IGF1R
0.882 0.200 15 98744146 intron variant T/C;G snv 5
rs13129697
SLC2A9
0.925 0.120 4 9925343 intron variant T/G snv 0.39 5
rs13197601
SLC17A1
0.882 0.200 6 25785707 intron variant G/A snv 0.32 5
rs174455
FADS3
1.000 0.080 11 61888645 intron variant G/A;C snv 5
rs1800977
ABCA1 ; LOC105376196
0.851 0.240 9 104928169 intron variant G/A;C snv 5
rs2070803
TRIM46
0.925 0.080 1 155185239 intron variant G/A snv 0.55 5
rs2199936
ABCG2
0.882 0.160 4 88124179 intron variant A/G;T snv 0.88 5
rs2762353
SLC17A1
0.882 0.200 6 25794203 intron variant A/G snv 0.66 5
rs3114020
ABCG2
0.882 0.200 4 88162514 intron variant T/C snv 0.40 5
rs3757131
SLC17A1
0.882 0.200 6 25783681 intron variant C/T snv 0.32 5
rs3799344
SLC17A1
0.882 0.200 6 25786765 intron variant C/T snv 0.41 5
rs4148155
ABCG2
0.882 0.200 4 88133515 intron variant A/G snv 8.7E-02 5
rs4481233
SLC2A9
0.925 0.120 4 9954455 intron variant C/T snv 0.16 5
rs4971100
TRIM46
0.925 0.120 1 155183255 intron variant G/A snv 0.39 5
rs62033406
FTO
16 53790314 intron variant A/G snv 0.33 5
rs626277
DACH1
1.000 0.080 13 71773564 intron variant A/C snv 0.51 5
rs733175
SLC2A9
0.851 0.240 4 10048517 intron variant C/T snv 0.77 5