Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10002268 1.000 0.080 4 55653725 intergenic variant T/C snv 0.41 1
rs10052657
PDE4D
0.807 0.120 5 59111944 intron variant C/A snv 0.17 7
rs10058728
CSNK1A1
1.000 0.080 5 149524529 intron variant A/T snv 0.64 2
rs10069690
TERT
0.595 0.560 5 1279675 intron variant C/T snv 0.36 53
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
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
rs10484761 0.807 0.080 6 40834522 intergenic variant T/C snv 0.31 7
rs104886003
PIK3CA
0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 71
rs104893819
TGFBR2
0.827 0.240 3 30688470 stop gained C/G;T snv 5
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
rs10786161
NOC3L
1.000 0.080 10 94347914 intron variant C/T snv 0.31 1
rs10821515
SYK
1.000 0.080 9 90862614 intron variant G/A;C snv 1
rs10842750
ITPR2
0.925 0.120 12 26537632 intron variant A/C;T snv 2
rs10882424
PLCE1 ; NOC3L
1.000 0.080 10 94326321 intron variant T/G snv 0.31 1
rs10882430
NOC3L ; PLCE1
1.000 0.080 10 94330915 3 prime UTR variant A/G snv 0.31 1
rs10931936
CASP8
0.827 0.120 2 201279205 intron variant T/C snv 0.72 6
rs11066001
BRAP
0.763 0.360 12 111681367 intron variant T/C snv 5.8E-03 15