Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9933544 0.882 0.040 16 24576962 downstream gene variant A/C snv 0.29 3
rs985033810
TP53
0.724 0.280 17 7674232 missense variant C/A;G;T snv 16
rs9642393
EGFR
0.925 0.040 7 55177954 intron variant T/C snv 0.24 2
rs942158624
TP53
0.724 0.320 17 7674948 missense variant T/A snv 19
rs8957
SLC2A4RG
0.925 0.040 20 63742354 missense variant G/T snv 0.71 0.78 2
rs891835
CCDC26
0.851 0.120 8 129479506 intron variant T/G snv 0.17 5
rs879254044
MSH2
0.925 0.040 2 47475148 missense variant G/A;C;T snv 3
rs878854066
TP53
0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs876660821
TP53
0.689 0.400 17 7675075 missense variant A/C;G;T snv 22
rs876659675
TP53
0.807 0.280 17 7674199 missense variant A/C;G;T snv 8
rs869320694
FGFR1
0.742 0.520 8 38414790 missense variant T/C snv 16
rs866987936
FBXW7
0.752 0.240 4 152326214 missense variant C/A;G;T snv 12
rs866960721
H3C4
0.851 0.040 6 26196856 missense variant C/G;T snv 4.0E-06 4
rs866775781
TP53
0.716 0.440 17 7675216 splice acceptor variant C/A;G snv 17
rs865880036
MEIS2
0.827 0.040 15 37098156 missense variant A/C snv 1.3E-04 5
rs864622237
TP53
0.716 0.320 17 7674263 missense variant A/C;G;T snv 17
rs863225401
MSH6 ; FBXO11
0.925 0.040 2 47799866 stop gained G/A snv 4
rs863224451
TP53
0.701 0.440 17 7673796 missense variant C/A;G;T snv 20
rs861539
KLC1 ; XRCC3
0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs833061
VEGFA
0.605 0.600 6 43769749 upstream gene variant C/G;T snv 42
rs8057643
RBFOX1
0.851 0.040 16 6910689 intron variant C/A;T snv 4
rs786205165
MTOR
0.882 0.120 1 11157173 missense variant C/A;T snv 4
rs786204929
PTEN
0.752 0.200 10 87933144 stop gained G/A;T snv 12
rs786201057
TP53
0.677 0.400 17 7675995 missense variant G/A;C;T snv 24
rs78378222
TP53
0.662 0.360 17 7668434 3 prime UTR variant T/G snv 8.3E-03 37