Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs28360317
XRCC4
0.716 0.280 5 83323739 intron variant -/CCT delins 0.24 15
rs104894360
KRAS
0.724 0.560 12 25209904 missense variant T/A;C snv 14
rs2075685
TMEM167A ; XRCC4
0.724 0.320 5 83076846 intron variant G/A;T snv 14
rs603965
CCND1
0.732 0.440 11 69648142 splice region variant G/A snv 14
rs874945 0.732 0.240 12 53961667 upstream gene variant C/T snv 0.38 14
rs2075686
TMEM167A ; XRCC4
0.742 0.240 5 83076927 intron variant C/T snv 1.7E-02 13
rs28931615
FGFR3
0.732 0.240 4 1804426 missense variant C/A;T snv 13
rs61330082
NAMPT
0.732 0.320 7 106286419 upstream gene variant G/A snv 0.22 13
rs861530
LOC112268131 ; XRCC3 ; KLC1
0.732 0.320 14 103707786 3 prime UTR variant T/C snv 0.65 13
rs1130214
AKT1
0.742 0.280 14 104793397 5 prime UTR variant C/A snv 0.31 12
rs1799794
XRCC3 ; KLC1
0.763 0.320 14 103712930 splice region variant T/C snv 0.22 12
rs3136817
APEX1 ; OSGEP
0.732 0.280 14 20456275 intron variant T/C snv 0.23 12
rs3757441
EZH2
0.752 0.200 7 148827660 intron variant C/T snv 0.80 12
rs3810366
ERCC2
0.732 0.280 19 45370684 5 prime UTR variant G/C;T snv 12
rs77191406
TNFAIP3
0.790 0.280 6 137881704 3 prime UTR variant C/T snv 7.2E-04 12
rs786204929
PTEN
0.752 0.200 10 87933144 stop gained G/A;T snv 12
rs8179090
TIMP2
0.752 0.280 17 78925807 upstream gene variant C/G snv 1.6E-02 12
rs10511729
LOC101929563
0.742 0.240 9 23557229 intron variant T/G snv 0.35 11
rs10811474 0.742 0.240 9 21114238 intergenic variant A/G snv 0.44 11
rs12683422
LINGO2
0.742 0.240 9 27969442 intron variant C/T snv 5.7E-02 11
rs4957014
AHRR ; PDCD6
0.752 0.160 5 287899 intron variant T/G snv 0.74 11
rs744154
ERCC4
0.763 0.280 16 13921224 intron variant G/C snv 0.23 11
rs776223836
ERCC2
0.763 0.280 19 45364045 missense variant G/A snv 11
rs12921862
AXIN1
0.763 0.200 16 331927 intron variant C/A snv 0.18 10
rs2155209
MRE11
0.776 0.240 11 94417624 3 prime UTR variant T/C snv 0.27 10