Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1353759920
TP73
0.851 0.120 1 3707593 missense variant C/A snv 2.1E-05 4
rs121908689
RAD54L ; LRRC41
0.925 0.120 1 46272758 missense variant T/A snv 2
rs121909775
CASP10
1.000 0.120 2 201205929 stop gained C/A;T snv 4.0E-06 2
rs28936699
CASP10
1.000 0.120 2 201209388 missense variant C/T snv 1
rs398122800
CASP10
1.000 0.120 2 201209189 frameshift variant -/A ins 1
rs267601395
EZH2
0.925 0.160 7 148811636 missense variant A/G;T snv 7
rs75002266
ORC4
0.827 0.160 2 147939241 missense variant G/A snv 3.2E-03 3.0E-03 6
rs1057519952
RHOA
0.882 0.160 3 49375577 missense variant G/A snv 5
rs2070673
LOC107984284 ; CYP2E1
0.827 0.160 10 133527063 non coding transcript exon variant A/T snv 0.67 5
rs1057519954
RHOA
0.882 0.160 3 49375465 missense variant T/A;C;G snv 4
rs1057519894
EZH2
0.925 0.160 7 148811650 missense variant T/A;G snv 2
rs13706
CDC6
0.776 0.200 17 40300899 missense variant G/A;C snv 0.15; 8.0E-06 11
rs2305160
NPAS2 ; NPAS2-AS1
0.776 0.200 2 100974842 missense variant A/G snv 0.71 0.75 9
rs1057519953
RHOA
0.807 0.200 3 49375576 missense variant C/A;T snv 8
rs267601394
EZH2
0.807 0.200 7 148811635 missense variant T/A;G snv 8
rs756091827
MYC ; CASC11
0.851 0.200 8 127738435 missense variant C/G;T snv 6
rs1057519918
CASC11 ; MYC
0.851 0.200 8 127738390 missense variant C/T snv 5
rs750664148
CASC11 ; MYC
0.851 0.200 8 127738434 missense variant A/C;G snv 5
rs1057519941
PIK3CA
0.776 0.240 3 179203761 missense variant T/C;G snv 10
rs398122820
B2M
0.790 0.240 15 44715641 missense variant G/A snv 8
rs1057519909
MAP2K1
0.790 0.240 15 66435116 missense variant A/C snv 7
rs63750042
MSH2
0.925 0.240 2 47408415 stop gained C/G;T snv 4.0E-06 6
rs760228510
PMS2
0.925 0.240 7 5999182 stop gained G/A;C snv 6
rs34767364
NBN
0.701 0.280 8 89971232 missense variant G/A;C snv 2.5E-03 20
rs2167270
LEP
0.724 0.280 7 128241296 5 prime UTR variant G/A snv 0.37 17