Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3219493
MUTYH
0.882 0.120 1 45330597 intron variant G/C snv 0.92 0.93 3
rs833052 0.827 0.160 6 43755598 intergenic variant A/C snv 0.88 5
rs2854509
XRCC1
0.807 0.160 19 43570445 intron variant T/G snv 0.80 6
rs3757441
EZH2
0.752 0.200 7 148827660 intron variant C/T snv 0.80 12
rs798766
TACC3
0.851 0.120 4 1732512 intron variant T/C snv 0.76 6
rs4957014
AHRR ; PDCD6
0.752 0.160 5 287899 intron variant T/G snv 0.74 11
rs4969054
SLC39A11
0.882 0.120 17 73016334 intron variant G/C snv 0.73 3
rs887569
EZH2
0.882 0.120 7 148808210 intron variant C/T snv 0.73 5
rs2157719
CDKN2B-AS1
0.708 0.360 9 22033367 non coding transcript exon variant C/T snv 0.71 17
rs25487
XRCC1
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs1495741 0.827 0.240 8 18415371 regulatory region variant G/A snv 0.71 9
rs2910164
MIR3142HG ; MIR146A
0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs2070744
NOS3
0.608 0.680 7 150992991 intron variant C/T snv 0.70 54
rs1805105
AXIN1
0.776 0.280 16 346264 synonymous variant A/G snv 0.61 0.69 11
rs11077654
SLC39A11
0.882 0.120 17 73010373 intron variant A/C snv 0.69 3
rs2010963
VEGFA
0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 82
rs762551
CYP1A2
0.701 0.400 15 74749576 intron variant C/A snv 0.67 23
rs7003908
PRKDC
0.716 0.320 8 47858141 intron variant C/A snv 0.66 16
rs2228001
XPC
0.570 0.480 3 14145949 missense variant G/T snv 0.63 0.65 60
rs861530
LOC112268131 ; XRCC3 ; KLC1
0.732 0.320 14 103707786 3 prime UTR variant T/C snv 0.65 13
rs1883965
MTOR
0.807 0.160 1 11262099 intron variant A/G snv 0.63 8
rs4813953
LINC02871
1.000 0.120 20 11010490 intron variant T/C snv 0.63 1
rs10775480
LOC105372093 ; SLC14A1
0.882 0.120 18 45737317 intron variant T/C snv 0.61 3
rs7238033
SLC14A1 ; LOC105372093
0.925 0.120 18 45737001 intron variant T/C snv 0.61 2
rs3213255
XRCC1
0.882 0.120 19 43573355 intron variant G/A snv 0.60 3