Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121909224
PTEN
0.627 0.560 10 87933147 stop gained C/G;T snv 1.2E-05 41
rs121909231
PTEN
0.667 0.600 10 87961095 stop gained C/A;T snv 32
rs121909218
PTEN
0.672 0.360 10 87933145 missense variant G/A snv 25
rs121909219
PTEN
0.689 0.400 10 87957915 stop gained C/A;T snv 25
rs121909229
PTEN
0.683 0.400 10 87933148 missense variant G/A;C;T snv 23
rs121913293
PTEN
0.732 0.360 10 87952142 missense variant C/A;T snv 18
rs587776667
PTEN
0.742 0.280 10 87931090 splice donor variant G/A;C;T snv 14
rs863224909
PTEN
0.732 0.360 10 87960952 stop gained C/A;G snv 14
rs121909222
PTEN
0.742 0.240 10 87933127 missense variant A/G snv 13
rs370795352
PTEN
0.742 0.360 10 87933163 missense variant T/A;C snv 4.0E-06 13
rs1085308041
PTEN
0.763 0.160 10 87965285 splice acceptor variant A/C;G snv 12
rs1085308043
PTEN
0.763 0.200 10 87925511 splice acceptor variant A/G;T snv 12
rs1224040268
PTEN
0.742 0.360 10 87931091 splice donor variant T/A;C snv 7.0E-06 12
rs1064793345
PTEN
0.752 0.240 10 87961039 missense variant T/C snv 11
rs876661024
PTEN
0.776 0.200 10 87957852 splice acceptor variant G/A;C;T snv 11
rs121909232
PTEN
0.776 0.160 10 87952258 stop gained C/A;G snv 4.0E-06 9
rs398123318
PTEN
0.776 0.240 10 87925558 splice region variant AGTA/- delins 9
rs587782350
PTEN
0.776 0.160 10 87957955 missense variant C/T snv 9
rs786201041
PTEN
0.776 0.160 10 87961119 splice donor variant G/A;C snv 9
rs1060500126
PTEN
0.790 0.160 10 87933223 missense variant A/C;G snv 8
rs1114167621
PTEN
0.790 0.160 10 87931045 splice acceptor variant G/A;C;T snv 8
rs1114167622
PTEN
0.790 0.160 10 87952260 splice donor variant G/C snv 8
rs1114167640
PTEN
0.790 0.160 10 87961067 stop gained TGACAAAGCAAATA/CGCTT delins 8
rs1114167650
PTEN
0.790 0.160 10 87925562 splice region variant G/A snv 8
rs121909223
PTEN
0.790 0.160 10 87933129 missense variant T/C;G snv 8