Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1435047610
CDK16
1.000 0.120 X 47223642 missense variant G/A snv 9.5E-06 1
rs770380303
MAP3K14
1.000 0.120 17 45289251 missense variant C/G snv 8.0E-06 1
rs1361241029
PBK
1.000 0.120 8 27828154 start lost T/C snv 2.1E-05 1
rs138280963
PRKACG
1.000 0.120 9 69013990 missense variant C/T snv 4.8E-05 2.0E-04 1
rs1370376642
RNF157-AS1 ; FOXJ1
1.000 0.120 17 76140095 missense variant G/A snv 1
rs12051350
SMG1
1.000 0.120 16 18896946 missense variant C/T snv 3.7E-02 1.5E-02 1
rs764152905
SMG1
1.000 0.120 16 18854890 missense variant T/A;C snv 8.0E-06; 2.4E-05 1
rs730881394
ATM ; C11orf65
0.925 0.320 11 108310222 missense variant C/T snv 4.0E-06 7.0E-06 2
rs1383461329
KMT5A
1.000 0.120 12 123389469 missense variant C/T snv 1.4E-05 2
rs773379832
SETX
0.925 0.320 9 132297011 missense variant A/G snv 1.2E-05 7.0E-06 2
rs876658923
EPM2AIP1 ; MLH1
1.000 0.120 3 36993593 frameshift variant TGAACCG/- delins 3
rs1057519910
MAP2K2
0.851 0.160 19 4117551 missense variant A/C;T snv 4
rs1057519958
RXRA
0.851 0.200 9 134436505 missense variant C/A;T snv 4
rs1057519919
MYCNOS ; MYCN
0.851 0.160 2 15942195 missense variant C/T snv 5
rs1057519944
POLE
0.882 0.160 12 132676599 missense variant G/A snv 5
rs750040814
XPC
0.827 0.160 3 14158639 missense variant C/T snv 1.6E-05 5.6E-05 5
rs121434498
MAP2K2
0.807 0.280 19 4117553 missense variant A/C;G;T snv 6
rs202003805
PRSS1
0.827 0.120 7 142750561 missense variant C/T snv 9.0E-05 6
rs1057519962
SMAD4
0.827 0.160 18 51067035 missense variant G/A;T snv 6
rs1057519882
CDKN2A
0.807 0.200 9 21974678 missense variant C/A snv 7
rs587778883
MLH1
0.807 0.200 3 37025648 frameshift variant A/- del 7
rs1057519960
SF3B2
0.827 0.280 11 66063413 missense variant A/G snv 7
rs121912580
SMAD4
0.807 0.280 18 51067036 missense variant G/A;C;T snv 7
rs1057519881
CDKN2A
0.776 0.240 9 21971111 missense variant T/C snv 8
rs121909235
PTEN
0.851 0.240 10 87957919 missense variant G/A snv 8