Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs67164370
RASSF2
0.851 0.120 20 4787830 intron variant -/AGGGACT ins 4
rs3783553
IL1A
0.667 0.480 2 112774138 3 prime UTR variant -/TGAA delins 26
rs144848
BRCA2
0.653 0.440 13 32332592 missense variant A/C snv 0.28 0.23 29
rs61764370
KRAS
0.662 0.320 12 25207290 3 prime UTR variant A/C snv 6.2E-02 29
rs314276
LIN28B
0.807 0.280 6 104960124 intron variant A/C snv 0.65 10
rs4987208
RAD52
0.851 0.160 12 913403 stop gained A/C snv 3.5E-02 2.1E-02 4
rs2256787
ARHGEF10L
0.925 0.120 1 17566321 intron variant A/C snv 0.93 2
rs115344852
GPX6
1.000 0.120 6 28518321 intron variant A/C snv 1
rs1614627 1.000 0.120 1 20620263 downstream gene variant A/C snv 0.86 1
rs854560
PON1
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs2032582
ABCB1
0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 97
rs2072590
HAGLR ; HAGLROS
0.851 0.120 2 176177905 non coding transcript exon variant A/C;T snv 4
rs17329882
SYNPO2
0.925 0.120 4 119028805 intron variant A/C;T snv 2
rs76032516
MAML2
0.925 0.120 11 96097550 intron variant A/C;T snv 2
rs1695
GSTP1
0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs5498
ICAM4 ; ICAM1
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs1128503
ABCB1
0.564 0.760 7 87550285 synonymous variant A/G snv 0.54 0.63 64
rs768623239
GSTM1 ; GSTM2
0.662 0.640 1 109689278 missense variant A/G snv 1.5E-05 26
rs851797
EXO1
0.752 0.240 1 241889740 3 prime UTR variant A/G snv 0.72 13
rs2070074
GALT
0.742 0.360 9 34649445 missense variant A/G snv 9.2E-02 7.4E-02 12
rs17401966
KIF1B
0.790 0.280 1 10325413 intron variant A/G snv 0.24 7
rs11782652
CHMP4C
0.851 0.120 8 81741409 intron variant A/G snv 6.6E-02 4
rs9303542
SKAP1
0.882 0.120 17 48334138 intron variant A/G snv 0.34 3
rs1057156
RUVBL1
0.925 0.120 3 128081228 3 prime UTR variant A/G snv 0.22 0.23 2