Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1052133
OGG1 ; CAMK1
0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs13181
KLC3 ; ERCC2
0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs7003908
PRKDC
0.716 0.320 8 47858141 intron variant C/A snv 0.66 16
rs13010627
CASP10
0.807 0.280 2 201209375 missense variant G/A snv 4.2E-02 4.3E-02 10
rs2227310
CASP7
0.807 0.160 10 113729393 missense variant C/G snv 0.26 0.23 9
rs751144688
CD44
1.000 0.080 11 35206195 missense variant C/T snv 4.0E-06 4
rs511044
CASP5
0.925 0.120 11 105024783 upstream gene variant T/C snv 3
rs12360870
MRE11
1.000 0.080 11 94440881 intron variant T/C snv 0.16 1