Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs745934102
PDPN
0.882 0.040 1 13607281 missense variant G/A snv 3.2E-05 1.4E-05 5
rs1057519757
PIK3R1
0.882 0.120 5 68293310 missense variant G/A;C snv 5
rs1057519841
PIK3R1
0.925 0.120 5 68295269 missense variant A/G snv 5
rs771563543
ZEB1
0.851 0.040 10 31510841 missense variant G/A snv 4.0E-06 1.4E-05 5
rs1872328
ACYP2
0.827 0.120 2 54168122 intron variant G/A snv 7.3E-02 6
rs1800435
ALAD
0.827 0.200 9 113391611 missense variant C/G snv 8.3E-02 6.1E-02 7
rs773442580
EGF
0.851 0.080 4 109913367 missense variant T/C;G snv 4.0E-06 7
rs149840192
EGFR
0.807 0.080 7 55154129 missense variant C/A;T snv 7
rs1057519906
IDH2
0.882 0.120 15 90088607 missense variant T/A;C snv 8
rs121909235
PTEN
0.851 0.240 10 87957919 missense variant G/A snv 8
rs876659675
TP53
0.807 0.280 17 7674199 missense variant A/C;G;T snv 8
rs1052576
CASP9
0.807 0.200 1 15506048 missense variant T/A;C snv 0.53 9
rs1057519995
TP53
0.807 0.240 17 7674200 missense variant T/A snv 9
rs11568821
LOC105373977 ; PDCD1
0.827 0.200 2 241851760 intron variant C/G;T snv 10
rs1057519926
PIK3CA
0.776 0.200 3 179210293 missense variant A/T snv 10
rs1057519986
TP53
0.776 0.240 17 7673811 missense variant A/C;G snv 10
rs1057519987
TP53
0.776 0.280 17 7673810 missense variant A/C snv 10
rs1057519988
TP53
0.776 0.240 17 7673812 missense variant A/C;G;T snv 10
rs371409680
TP53
0.790 0.120 17 7673772 missense variant C/G;T snv 4.0E-05 7.0E-06 10
rs397516896
BRAF
0.763 0.360 7 140753355 missense variant C/G;T snv 11
rs80357796
BRCA1
0.752 0.240 17 43094464 frameshift variant T/- del 11
rs1057519933
PIK3CA
0.790 0.240 3 179199156 missense variant A/G snv 11
rs1057519934
PIK3CA
0.790 0.240 3 179199158 missense variant G/C snv 11
rs1057519935
PIK3CA
0.790 0.240 3 179199157 missense variant A/G snv 11
rs1057519936
PIK3CA
0.776 0.200 3 179234284 missense variant A/G;T snv 11