Source: CURATED ×
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
rs863224909
PTEN
0.732 0.360 10 87960952 stop gained C/A;G snv 14
rs370795352
PTEN
0.742 0.360 10 87933163 missense variant T/A;C snv 4.0E-06 13
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 10
rs121909227
PTEN
0.776 0.240 10 87957858 stop gained C/T snv 8
rs1057519368
PTEN
0.882 0.320 10 87957958 stop gained T/A;C;G snv 4.0E-06 4
rs1114167667
PTEN
0.925 0.240 10 87961051 stop gained T/A;G snv 3
rs797045904
PTEN
0.925 0.240 10 87960992 frameshift variant C/- del 3
rs121909238
PTEN
0.925 0.240 10 87933037 missense variant A/C;G snv 2
rs121909239
PTEN
0.925 0.240 10 87957973 missense variant A/G;T snv 2
rs121909240
PTEN
0.925 0.240 10 87957940 missense variant T/C snv 2
rs397514559
PTEN
0.925 0.240 10 87952125 missense variant C/A snv 2
rs397514560
PTEN
0.925 0.240 10 87933151 missense variant C/G;T snv 2
rs398123323
PTEN
1.000 0.200 10 87933163 frameshift variant -/A delins 2
rs1564568303
PTEN
1.000 0.200 10 87960957 frameshift variant -/GA delins 1
rs797045066
PTEN
1.000 0.200 10 87965303 frameshift variant -/A delins 1
rs1057524874
PTEN ; KLLN
1.000 0.200 10 87864510 frameshift variant -/GA delins 1