Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs16986825
ZNRF3
1.000 0.120 22 28904318 intron variant C/T snv 0.13 1
rs4285214
ZNF608
1.000 0.120 5 124688588 intron variant T/G snv 0.55 1
rs3218536
XRCC2
0.620 0.440 7 152648922 missense variant C/G;T snv 4.0E-06; 6.4E-02 37
rs25487
XRCC1
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs1799782
XRCC1
0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs25489
XRCC1
0.550 0.720 19 43552260 missense variant C/G;T snv 8.5E-06; 7.1E-02 78
rs139599857
XRCC1
0.882 0.120 19 43545922 missense variant C/G snv 1.6E-05 2.1E-05 3
rs2607775
XPC ; LSM3
0.807 0.160 3 14178595 5 prime UTR variant C/G snv 0.42 0.43 8
rs3731055
XPC ; LSM3
0.925 0.120 3 14178939 intron variant C/T snv 1.9E-02 2
rs2470353
XPC ; LOC107986063
0.925 0.120 3 14148768 intron variant G/A;C;T snv 0.41; 1.5E-04 2
rs2228000
XPC
0.585 0.560 3 14158387 missense variant G/A snv 0.24 0.21 53
rs3729587
XPC
0.925 0.120 3 14167125 intron variant G/C snv 0.31 0.34 2
rs3731114
XPC
0.925 0.120 3 14165122 intron variant C/G snv 1.8E-02 2
rs11644322
WWOX
0.925 0.120 16 79005703 intron variant C/T snv 0.22 3
rs351365
WNT2B
1.000 0.120 1 112503773 intron variant T/C;G snv 1
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs2239186
VDR
0.882 0.120 12 47875627 intron variant A/C;G snv 0.17 5
rs145733073
UGT1A8 ; UGT1A9 ; UGT1A7 ; UGT1A10
0.925 0.120 2 233682175 missense variant T/C;G snv 4.0E-06; 1.4E-04 2
rs2235108
TRIB1
0.925 0.120 8 125436547 3 prime UTR variant G/A snv 0.25 3
rs2980874
TRIB1
0.925 0.120 8 125432546 intron variant G/A snv 0.30 2
rs7074891
TRDMT1
0.925 0.120 10 17146475 3 prime UTR variant C/T snv 0.95 2
rs935821839
TP73
0.925 0.120 1 3727199 missense variant A/G snv 7.0E-06 2
rs949647240
TP73
0.925 0.120 1 3707693 missense variant C/T snv 2
rs9854771
TP63
0.925 0.240 3 189790682 intron variant G/A snv 0.34 2