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
rs13181
KLC3 ; ERCC2
0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs1136410
PARP1
0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70
rs759412116
ERCC2
0.581 0.640 19 45352210 missense variant C/G;T snv 4.0E-06; 6.0E-05 55
rs156697
GSTO2
0.672 0.560 10 104279427 missense variant A/G;T snv 0.35 25
rs4925
GSTO1
0.677 0.560 10 104263031 missense variant C/A snv 0.25 0.23 28
rs1346044
WRN
0.708 0.440 8 31167138 missense variant T/C snv 0.24 0.23 23
rs104894201
CRYAB
0.763 0.280 11 111908934 missense variant T/C snv 12
rs58596362
LMNA
0.827 0.280 1 156138613 splice region variant C/A;T snv 8.1E-06 7
rs79121622
HSF4
0.827 0.080 16 67165833 missense variant G/A snv 3.3E-04 9.8E-05 5
rs7278468
LOC107987300 ; CRYAA
0.882 0.280 21 43168647 upstream gene variant T/A;G snv 3
rs1190613858
LMNA
0.925 0.120 1 156139085 synonymous variant C/T snv 4.0E-06 3
rs3754334
EPHA2
0.925 0.040 1 16125272 synonymous variant G/A snv 0.28 0.24 2
rs1052559
KLC3 ; ERCC2
1.000 0.040 19 45351661 stop gained T/A;G snv 2