Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121434592
AKT1
0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 54
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs121912665
TP53
1.000 0.120 17 7674965 missense variant G/A snv 2.4E-05 7.0E-06 7
rs121913237
NRAS
0.611 0.560 1 114716126 missense variant C/A;G;T snv 8.0E-06 50
rs121913355
BRAF
0.641 0.520 7 140781602 missense variant C/A;G;T snv 4.0E-06 42
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs121913444
EGFR
0.724 0.160 7 55191831 missense variant T/A;C;G snv 18
rs121913465
EGFR ; EGFR-AS1
0.763 0.160 7 55181312 missense variant G/T snv 11
rs121913529
KRAS
0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 144
rs121913530
KRAS
0.583 0.640 12 25245351 missense variant C/A;G;T snv 63
rs121918464
PTPN11
0.708 0.440 12 112450406 missense variant G/A;C snv 25
rs12203582
IL17F
0.827 0.120 6 52240759 intron variant G/A;T snv 7
rs1227480017
RRM2
2 10122697 synonymous variant C/A snv 1
rs12296850 0.925 0.080 12 100426307 downstream gene variant A/G snv 8.7E-02 3
rs12541709
TNKS
1.000 0.080 8 9751081 intron variant C/G snv 0.29 2
rs125555
MBD1
0.882 0.080 18 50273809 missense variant G/A;C snv 3.6E-05; 0.19 4
rs12613347
CASP10
2 201190589 intron variant C/T snv 0.19 1
rs1289543302
ABCB1
0.763 0.440 7 87536472 missense variant C/T snv 12
rs1333049
CDKN2B-AS1
0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs1340420
TNKS2
0.925 0.080 10 91857549 intron variant A/G snv 0.71 0.70 3
rs1347093
LOC105374690 ; MIR217HG
0.882 0.080 2 56019205 intron variant G/T snv 0.21 4
rs1367644026
KRT5
0.925 0.080 12 52520259 missense variant C/A;T snv 4.0E-06 5
rs138895564
TERT
0.882 0.080 5 1271959 intron variant C/T snv 5.1E-03 4
rs1397529
GAB1
0.882 0.080 4 143471009 3 prime UTR variant A/C;T snv 4
rs139852726
LPCAT1
0.882 0.080 5 1462734 3 prime UTR variant G/A;C snv 4