Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7248488
ZNF208
0.851 0.160 19 22005907 intron variant A/C snv 0.59 5
rs8103163
ZNF208
0.882 0.120 19 21991950 intron variant A/C snv 0.59 4
rs9841504
ZBTB20
0.827 0.120 3 114643917 intron variant C/G;T snv 7
rs3747093
YDJC
0.732 0.200 22 21630090 upstream gene variant G/A snv 0.32 16
rs6869366
XRCC4 ; TMEM167A
0.701 0.280 5 83075927 intron variant T/G snv 9.2E-02 18
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
rs767551092
XPC
0.790 0.200 3 14164838 missense variant G/A snv 4.0E-06 10
rs756762196
WWOX
0.851 0.120 16 78425054 stop gained C/G;T snv 1.6E-05 4
rs583522
WAKMAR2 ; TNFAIP3
0.925 0.080 6 137868747 intron variant C/A;T snv 3
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs11568820
VDR
0.672 0.480 12 47908762 intron variant C/T snv 0.38 27
rs1989969
VDR
0.827 0.120 12 47884227 intron variant A/C;G;T snv 0.60 8
rs2107301
VDR
0.807 0.120 12 47861787 intron variant G/A snv 0.26 7
rs246079
UNG
0.790 0.120 12 109109255 intron variant A/G;T snv 9
rs353163
UBA6-AS1 ; TMPRSS11A
0.882 0.080 4 67919056 missense variant T/A;C;G snv 0.67 4
rs2244438
TRAK2
0.882 0.080 2 201387816 missense variant G/A;T snv 0.29; 4.0E-06 4
rs12231737
TRAFD1
0.925 0.120 12 112136812 intron variant C/T snv 5.9E-03 5
rs13054361
TPTEP2-CSNK1E
1.000 0.080 22 38336819 intron variant G/A snv 9.3E-02 1
rs7289981
TPTEP2-CSNK1E
1.000 0.080 22 38323957 intron variant C/T snv 0.18 1
rs1801173
TP73
0.851 0.120 1 3682346 5 prime UTR variant C/T snv 0.20 0.18 5
rs2273953
TP73
0.851 0.120 1 3682336 5 prime UTR variant G/A;T snv 0.20; 3.3E-04 5
rs1042522
TP53
0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1131691014
TP53
0.439 0.800 17 7676154 frameshift variant -/C ins 214