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
rs1057520009
XPO1
0.790 0.200 2 61492337 missense variant C/T snv 4.4E-06 14
rs1057520010
XPO1
0.882 0.200 2 61492336 missense variant T/A;G snv 5
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
rs1222213359
VEGFA
0.574 0.720 6 43770966 missense variant G/A snv 62
rs76316943
UTP23
0.790 0.080 8 116836068 intron variant G/A snv 1.3E-02 9
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
rs2186607
TRPC6
0.776 0.080 11 101785666 intron variant T/A snv 0.51 10
rs28934576
TP53
0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 78
rs11540652
TP53
0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 57
rs121912651
TP53
0.605 0.680 17 7674221 missense variant G/A;C snv 4.0E-06 53
rs121913343
TP53
0.611 0.520 17 7673803 missense variant G/A;C;T snv 1.2E-05 44
rs28934575
TP53
0.641 0.400 17 7674230 missense variant C/A;G;T snv 37
rs1057519975
TP53
0.649 0.480 17 7675209 missense variant A/C;G;T snv 34
rs121912666
TP53
0.645 0.360 17 7674872 missense variant T/C;G snv 8.0E-06 34