Source: UNIPROT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913315
STK11
0.882 0.160 19 1220488 missense variant G/A;T snv 2
rs137853080
STK11
1.000 0.040 19 1207058 missense variant T/G snv 1
rs137853081
STK11
1.000 0.040 19 1219352 missense variant G/C;T snv 1
rs387906659
AKT2
0.742 0.280 19 40257052 stop gained C/A;T snv 1
rs121913343
TP53
0.611 0.520 17 7673803 missense variant G/A;C;T snv 1.2E-05 1
rs200476704
TRAPPC1 ; CNTROB ; KCNAB3
1.000 0.040 17 7930659 stop gained G/A;C snv 2.4E-05 1
rs28934578
TP53
0.605 0.600 17 7675088 missense variant C/A;T snv 4.0E-06 1
rs762846821
TP53
0.614 0.320 17 7675151 missense variant C/A;T snv 8.0E-06 1
rs2066844
NOD2
0.587 0.520 16 50712015 missense variant C/T snv 2.6E-02 2.9E-02 2
rs121434592
AKT1
0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 2
rs397514644
AKT1
0.925 0.040 14 104780190 missense variant G/A snv 7.0E-06 1
rs861539
KLC1 ; XRCC3
0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 1
rs45580035
BRCA2
0.790 0.240 13 32380043 missense variant C/T snv 1.2E-05 1
rs80359204
BRCA2
1.000 0.040 13 32394741 missense variant A/G snv 1
rs121913530
KRAS
0.583 0.640 12 25245351 missense variant C/A;G;T snv 5
rs121913529
KRAS
0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 3
rs112445441
KRAS
0.658 0.400 12 25245347 missense variant C/A;G;T snv 2
rs104894340
CDK4
0.827 0.200 12 57751647 missense variant C/A;T snv 1
rs11547328
CDK4
0.701 0.360 12 57751648 missense variant G/A;T snv 4.0E-06 1
rs121913240
KRAS
0.672 0.440 12 25227342 missense variant T/A;C;G snv 1
rs104894230
HRAS ; LRRC56
0.564 0.600 11 534288 missense variant C/A;G;T snv 2
rs104894229
LRRC56 ; HRAS
0.564 0.600 11 534289 missense variant C/A;G;T snv 1
rs121913233
HRAS ; LRRC56
0.627 0.520 11 533874 missense variant T/A;C;G snv 1
rs121909233
KLLN ; PTEN
1.000 0.040 10 87864524 missense variant G/A snv 1
rs121909234
PTEN
1.000 0.040 10 87957867 missense variant G/A snv 1