Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12646351
ZNF827
0.790 0.080 4 145819473 intron variant G/A snv 0.19 10
rs17806780
ZNF827
0.790 0.080 4 145811502 intron variant T/C snv 0.18 10
rs704017
ZMIZ1-AS1
0.776 0.080 10 79059375 intron variant A/G snv 0.55 10
rs1250567
ZMIZ1
0.776 0.080 10 79286508 intron variant T/C snv 0.56 10
rs10511330
ZBTB20
0.776 0.080 3 114402172 intron variant T/C snv 0.22 10
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
rs760891242
XPC
0.925 0.080 3 14168309 missense variant G/C snv 4.0E-06 7.0E-06 3
rs1912804
WWOX
0.790 0.080 16 78592686 intron variant C/G;T snv 9
rs10506868
VTI1A
0.716 0.160 10 112559621 intron variant C/T snv 3.1E-02 16
rs12241008
VTI1A
0.716 0.160 10 112520943 intron variant T/C snv 0.13 16
rs12246635
VTI1A
0.776 0.080 10 112528860 intron variant T/C snv 0.13 10
rs12255141
VTI1A
0.790 0.080 10 112535133 intron variant A/G;T snv 9
rs2010963
VEGFA
0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 82
rs1222213359
VEGFA
0.574 0.720 6 43770966 missense variant G/A snv 62
rs1443465532
VEGFA
0.882 0.080 6 43774362 missense variant G/C snv 4.0E-06 7.0E-06 6
rs11832059
VDR
0.925 0.080 12 47879066 missense variant A/C;G snv 4.0E-06; 1.9E-03 2
rs76316943
UTP23
0.790 0.080 8 116836068 intron variant G/A snv 1.3E-02 9
rs1448674651
TYMS ; ENOSF1
0.667 0.560 18 671384 missense variant G/A;C snv 4.0E-06 23
rs11168936
TUBA1C
0.708 0.280 12 49251457 intron variant T/A;C snv 17
rs12144319
TTC22
0.776 0.080 1 54780362 3 prime UTR variant T/C snv 0.31 10
rs12143541
TTC22
0.790 0.080 1 54782179 intron variant A/G snv 0.11 9
rs187960998
TRPM1 ; MIR211
0.925 0.080 15 31065098 mature miRNA variant C/T snv 1.2E-05 6.3E-05 3
rs2186607
TRPC6
0.776 0.080 11 101785666 intron variant T/A snv 0.51 10