Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7726159
TERT
0.790 0.160 5 1282204 intron variant C/A snv 0.29 10
rs13428812
DNMT3A
0.827 0.120 2 25269598 intron variant A/G snv 0.31 9
rs246079
UNG
0.790 0.120 12 109109255 intron variant A/G;T snv 9
rs1989969
VDR
0.827 0.120 12 47884227 intron variant A/C;G;T snv 0.60 8
rs2303426
MSH2
0.790 0.080 2 47403411 intron variant C/A;G;T snv 1.9E-05; 0.47 8
rs3819102
ENOSF1
0.827 0.120 18 675307 intron variant A/G snv 4.5E-02 3.6E-02 8
rs41291957
CARMN ; MIR145 ; MIR143
0.882 0.200 5 149428827 intron variant G/A snv 0.12 7
rs6504950
STXBP4
0.807 0.120 17 54979110 intron variant G/A snv 0.29 7
rs7664413
VEGFC ; LOC105377555
0.851 0.160 4 176687553 intron variant C/T snv 0.24 0.25 7
rs798766
TACC3
0.851 0.120 4 1732512 intron variant T/C snv 0.76 6
rs9471643
PGC
0.882 0.080 6 41751177 intron variant G/C snv 0.19 6
rs4919743
KRT8
0.925 0.080 12 52915800 intron variant G/A snv 0.13 5
rs12740674
GNG12-AS1 ; WLS
0.882 0.080 1 68121775 intron variant C/T snv 0.34 4
rs13254990
PVT1
0.882 0.120 8 128064205 intron variant C/T snv 0.24 4
rs6458238
PGC
0.882 0.080 6 41749967 intron variant G/A;C snv 4
rs2001389
SUFU
0.925 0.120 10 102615501 intron variant G/A;C snv 3
rs2046463
LOC105377555
1.000 0.080 4 176681548 intron variant G/A;C snv 3
rs4635002
DOCK1
0.925 0.080 10 127064415 intron variant A/C snv 0.92 3
rs5999749
MAPK1
0.925 0.080 22 21833371 intron variant A/C;T snv 3
rs7853122
RAPGEF1
0.925 0.080 9 131705224 intron variant C/T snv 0.87 3
rs11777210
KBTBD11
1.000 0.080 8 1979843 intron variant C/G;T snv 2
rs1670661
NELL1
1.000 0.040 11 21209124 intron variant C/G;T snv 2
rs11646171
CDH8
16 61824185 intron variant G/A snv 0.13 1
rs169724
SYK
9 90828217 intron variant T/C;G snv 1
rs182361
SYK
9 90828077 intron variant C/A snv 0.11 1