Source: CLINVAR

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 35
rs121909231
PTEN
0.667 0.600 10 87961095 stop gained C/A;T snv 29
rs121909219
PTEN
0.689 0.400 10 87957915 stop gained C/A;T snv 24
rs121913293
PTEN
0.732 0.360 10 87952142 missense variant C/A;T snv 18
rs121909218
PTEN
0.672 0.360 10 87933145 missense variant G/A snv 14
rs587776667
PTEN
0.742 0.280 10 87931090 splice donor variant G/A;C;T snv 14
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
rs121913294
PTEN
0.776 0.280 10 87952143 missense variant G/A;C;T snv 8.0E-06 11
rs786204858
PTEN
0.776 0.280 10 87933079 missense variant A/G;T snv 11
rs876661024
PTEN
0.776 0.200 10 87957852 splice acceptor variant G/A;C;T snv 11
rs1064793345
PTEN
0.752 0.240 10 87961039 missense variant T/C snv 10
rs1085308046
PTEN
0.790 0.240 10 87933160 missense variant T/C;G snv 9
rs1085308045
PTEN
0.807 0.160 10 87933128 missense variant C/G;T snv 8
rs1085308056
PTEN
0.851 0.160 10 87957850 splice region variant C/G snv 8
rs1554893835
PTEN
0.827 0.240 10 87894110 splice donor variant G/C;T snv 8
rs398123316
PTEN
0.851 0.160 10 87925530 missense variant A/G;T snv 8
rs1085308050
PTEN
0.827 0.160 10 87933178 frameshift variant -/A delins 7
rs1085308054
PTEN
0.827 0.160 10 87952231 frameshift variant AT/- delins 7
rs1085308039
PTEN
0.925 0.080 10 87933075 stop gained G/T snv 6
rs1085308040
PTEN
0.851 0.200 10 87961096 missense variant G/A;T snv 6
rs1085308051
PTEN
0.882 0.200 10 87933229 missense variant A/G snv 4.0E-06 6
rs786202918
PTEN
0.925 0.080 10 87957951 stop gained C/T snv 4.0E-06 6
rs1085308047
PTEN ; KLLN
0.827 0.160 10 87864509 missense variant A/G snv 6
rs1085308052
PTEN
0.851 0.160 10 87952144 frameshift variant -/T delins 5