Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1173771 5 32814922 regulatory region variant A/G snv 0.65 9
rs459193
C5orf67
0.925 0.120 5 56510924 downstream gene variant A/G snv 0.69 9
rs445
CDK6
7 92779056 intron variant C/T snv 0.14 9
rs45446698
CYP3A7-CYP3A51P ; CYP3A7 ; ZSCAN25
0.807 0.120 7 99735325 upstream gene variant T/G snv 2.7E-02 9
rs6457374
HLA-B ; LOC112267902
0.851 0.200 6 31304484 intron variant C/T snv 0.81 9
rs11205303
MTMR11
0.882 0.120 1 149934520 missense variant T/C snv 0.33 0.29 9
rs12967135 18 60181790 intergenic variant G/A snv 0.24 8
rs2145272 20 6645571 intergenic variant G/A;T snv 8
rs34811474
ANAPC4
1.000 0.040 4 25407216 missense variant G/A;T snv 0.15; 4.1E-06 8
rs1966265
FGFR4
0.827 0.160 5 177089630 missense variant G/A;T snv 0.25 8
rs2011077
FGFR4
0.807 0.080 5 177094455 intron variant C/T snv 0.19 8
rs1182188
GNA12
0.827 0.120 7 2830351 intron variant T/C snv 0.26 8
rs110419
LOC105376536 ; LMO1
0.827 0.200 11 8231306 intron variant A/G snv 0.42 8
rs6234
PCSK1 ; LOC101929710
0.851 0.160 5 96393270 missense variant G/C snv 0.27 0.24 8
rs3823418
PSORS1C1
0.925 0.120 6 31133165 intron variant G/A snv 0.23 8
rs35874463
SMAD3
0.827 0.120 15 67165360 missense variant A/G snv 4.0E-02 3.4E-02 8
rs2066808
STAT2
0.807 0.280 12 56344189 intron variant A/G snv 0.21 8
rs16948048
ZNF652 ; LOC102724596
0.925 0.040 17 49363104 intron variant A/G snv 0.37 8
rs13437082 1.000 6 31386783 upstream gene variant C/T snv 0.32 7
rs33912345
C14orf39 ; SIX6
0.807 0.200 14 60509819 missense variant C/A;G snv 0.53 7
rs7203984
CETP
16 56965346 intron variant A/C snv 0.31 7
rs34517439
DNAJB4 ; GIPC2
0.882 0.120 1 77984833 intron variant C/A snv 7.3E-02 7
rs6024836
FAM210B ; AURKA
0.851 0.160 20 56369012 downstream gene variant G/A snv 0.42 7
rs13108218
HGFAC
4 3442204 intron variant A/G;T snv 7
rs7689420
HHIP-AS1 ; HHIP
0.851 0.080 4 144647200 non coding transcript exon variant T/C snv 0.79 7