Gene: PTEN ×
Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1085308040
rs1085308040
PTEN
6 0.851 0.200 10 87961096 missense variant G/A;T snv 0.700 0
dbSNP: rs1085308041
rs1085308041
PTEN
12 0.763 0.160 10 87965285 splice acceptor variant A/C;G snv 0.700 0
dbSNP: rs1085308042
rs1085308042
PTEN
4 0.882 0.120 10 87894076 missense variant G/A snv 0.700 0
dbSNP: rs1085308044
rs1085308044
PTEN ; KLLN
5 0.882 0.120 10 87864504 missense variant A/C snv 0.700 0
dbSNP: rs1085308045
rs1085308045
PTEN
8 0.807 0.160 10 87933128 missense variant C/G;T snv 0.700 0
dbSNP: rs1085308046
rs1085308046
PTEN
9 0.790 0.240 10 87933160 missense variant T/C;G snv 0.700 0
dbSNP: rs1085308047
rs1085308047
PTEN ; KLLN
6 0.827 0.160 10 87864509 missense variant A/G snv 0.700 0
dbSNP: rs1085308049
rs1085308049
PTEN
3 0.925 0.080 10 87957885 stop gained A/T snv 0.700 0
dbSNP: rs1085308050
rs1085308050
PTEN
7 0.827 0.160 10 87933178 frameshift variant -/A delins 0.700 0
dbSNP: rs1085308052
rs1085308052
PTEN
5 0.851 0.160 10 87952144 frameshift variant -/T delins 0.700 0
dbSNP: rs1085308053
rs1085308053
PTEN
5 0.882 0.080 10 87952230 missense variant C/T snv 0.700 0
dbSNP: rs1085308054
rs1085308054
PTEN
7 0.827 0.160 10 87952231 frameshift variant AT/- delins 0.700 0
dbSNP: rs1085308055
rs1085308055
PTEN
4 0.882 0.120 10 87952240 frameshift variant TCAGT/- delins 0.700 0
dbSNP: rs121909224
rs121909224
PTEN
41 0.627 0.560 10 87933147 stop gained C/G;T snv 1.2E-05 0.700 0
dbSNP: rs121913294
rs121913294
PTEN
14 0.776 0.280 10 87952143 missense variant G/A;C;T snv 8.0E-06 0.700 0
dbSNP: rs398123316
rs398123316
PTEN
9 0.851 0.160 10 87925530 missense variant A/G;T snv 0.700 0
dbSNP: rs786202918
rs786202918
PTEN
6 0.925 0.080 10 87957951 stop gained C/T snv 4.0E-06 0.700 0
dbSNP: rs786204875
rs786204875
PTEN
4 0.882 0.120 10 87960913 stop gained G/A;T snv 0.700 0
dbSNP: rs876660634
rs876660634
PTEN
10 0.807 0.200 10 87925551 missense variant A/C;G snv 0.700 0