Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2280148
SOCS3
0.925 0.080 17 78358299 3 prime UTR variant T/G snv 2.5E-02 2
rs776977530
TMED7-TICAM2 ; TMED7
0.925 0.160 5 115625723 synonymous variant G/A snv 4.6E-06 2
rs1567549584
TP53
0.925 0.120 17 7674245 missense variant T/C snv 2
rs7834169 0.925 0.120 8 27052774 upstream gene variant C/G snv 0.16 3
rs2238151
ALDH2
1.000 0.040 12 111774029 intron variant T/C snv 0.52 3
rs2032809
BBC3
0.882 0.120 19 47232959 upstream gene variant T/C snv 0.66 3
rs2742976
E2F2
0.882 0.240 1 23531510 upstream gene variant T/A;G snv 3
rs1057519830
EGFR
1.000 0.040 7 55163737 missense variant C/T snv 3
rs1057519887
EGFR
0.925 0.040 7 55154128 missense variant GC/AA;AT mnv 3
rs769696078
EGFR
0.925 0.040 7 55154128 missense variant G/A snv 3
rs1380228918
ERCC2
1.000 0.040 19 45364065 synonymous variant C/T snv 3
rs2237025
KIT
0.882 0.080 4 54675713 intron variant T/C snv 0.60 3
rs11599672
LOC105378438 ; PLCE1
0.925 0.080 10 93993019 regulatory region variant T/G snv 0.21 3
rs3810294
MIR3191 ; BBC3
0.882 0.120 19 47228572 intron variant C/T snv 0.14 3
rs1211098985
MTRR
1.000 0.040 5 7878128 missense variant T/C;G snv 4.0E-06 3
rs139994842
NOTCH1
0.925 0.040 9 136508308 missense variant G/A;C snv 1.5E-03 3
rs1052823
TNFAIP2
1.000 0.040 14 103137233 3 prime UTR variant G/A;C;T snv 0.15 3
rs1052912
TNFAIP2
1.000 0.040 14 103137316 3 prime UTR variant G/A snv 0.13 3
rs710100
TNFAIP2
1.000 0.040 14 103135941 missense variant A/G snv 0.64 0.59 3
rs1064793881
TP53
0.925 0.120 17 7673784 missense variant C/T snv 3
rs876659477
TP53
0.882 0.040 17 7673730 missense variant T/C snv 3
rs4663402
ATG16L1
0.851 0.080 2 233285017 intron variant A/T snv 5.1E-02 4
rs1049253
CASP3
0.851 0.160 4 184627797 3 prime UTR variant A/G snv 0.13 4
rs3213180
E2F1 ; NECAB3
0.925 0.120 20 33675818 3 prime UTR variant G/C snv 7.6E-02 4
rs1276184054
EGFR
0.851 0.080 7 55201305 missense variant G/A snv 4.0E-06 4