Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs25487
XRCC1
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs1052133
OGG1 ; CAMK1
0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs11615
ERCC1
0.572 0.640 19 45420395 synonymous variant A/G snv 0.50 0.55 62
rs1800566
NQO1
0.576 0.680 16 69711242 missense variant G/A snv 0.25 0.21 59
rs243865
MMP2
0.600 0.640 16 55477894 intron variant C/T snv 0.19 48
rs3212986
CD3EAP ; ERCC1
0.620 0.400 19 45409478 stop gained C/A;G;T snv 0.29; 4.3E-06; 4.3E-06 42
rs1001179
CAT
0.641 0.680 11 34438684 upstream gene variant C/T snv 0.16 33
rs121907906
WT1
0.776 0.320 11 32392717 stop gained G/A snv 8
rs869025212
BAP1
0.827 0.200 3 52403428 frameshift variant G/- delins 6
rs746965070
NBN
0.827 0.200 8 89955487 missense variant T/C snv 1.2E-05 5
rs1049305
AQP1
0.925 0.160 7 30924207 3 prime UTR variant G/C snv 0.52 4
rs17338032
CRTAM
1.000 0.080 11 122862895 intron variant G/T snv 1