Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10069690
TERT
0.595 0.560 5 1279675 intron variant C/T snv 0.36 53
rs10088262
LOC105375739
0.925 0.160 8 123753462 intergenic variant A/G snv 0.56 2
rs1014867
FAT4
0.925 0.080 4 125491736 missense variant C/T snv 4.9E-02 4.9E-02 3
rs1035142
FLACC1
0.807 0.200 2 201288355 3 prime UTR variant T/C;G snv 0.54 7
rs1039808
FAT4
0.925 0.080 4 125318831 missense variant C/G;T snv 4.0E-06; 0.41 3
rs1042522
TP53
0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs10437048
PADI4
1.000 0.080 1 17356224 intron variant A/C snv 1
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs1047972
AURKA
0.716 0.240 20 56386407 missense variant T/C snv 0.85 0.84 19
rs104886003
PIK3CA
0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 71
rs104894229
LRRC56 ; HRAS
0.564 0.600 11 534289 missense variant C/A;G;T snv 73
rs104894230
HRAS ; LRRC56
0.564 0.600 11 534288 missense variant C/A;G;T snv 73
rs1048943
CYP1A1
0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 88
rs10509670
PLCE1
0.851 0.080 10 94308190 intron variant A/G snv 0.30 5
rs1051740
EPHX1
0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27 56
rs1052133
OGG1 ; CAMK1
0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs1057519747
TP53
0.716 0.280 17 7675094 missense variant A/C;G;T snv 23
rs1057519883
CDKN2A
0.742 0.280 9 21971120 missense variant C/G;T snv 14
rs1057519886
CTNNB1
0.752 0.240 3 41224609 missense variant T/A;C;G snv 11
rs1057519889
EP300
0.807 0.200 22 41169525 missense variant G/A;T snv 6
rs1057519895
FBXW7
0.724 0.240 4 152328232 missense variant C/A;G;T snv 17
rs1057519896
FBXW7
0.742 0.320 4 152326136 missense variant C/A;T snv 12
rs1057519900
FGFR2
0.882 0.120 10 121515259 missense variant C/T snv 3
rs1057519918
CASC11 ; MYC
0.851 0.200 8 127738390 missense variant C/T snv 5
rs1057519927
PIK3CA
0.716 0.240 3 179218295 missense variant A/C;G;T snv 19