Source: CLINVAR ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1085308041
PTEN
0.763 0.160 10 87965285 splice acceptor variant A/C;G snv 12
rs121909232
PTEN
0.776 0.160 10 87952258 stop gained C/A;G snv 4.0E-06 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
rs121909225
PTEN
0.790 0.160 10 87894049 missense variant T/C;G snv 8
rs121909241
PTEN
0.790 0.160 10 87933154 missense variant G/A;T snv 8
rs138336847
PTEN
0.790 0.160 10 87952264 splice region variant G/A;C snv 4.0E-06 8
rs398123317
PTEN
0.790 0.160 10 87925550 missense variant T/A;C;G snv 8
rs587781784
PTEN
0.790 0.160 10 87952116 splice acceptor variant A/C;G;T snv 8
rs587782350
PTEN
0.776 0.160 10 87957955 missense variant C/T snv 8
rs587782455
PTEN
0.790 0.160 10 87960892 splice acceptor variant A/G;T snv 5.1E-05 8
rs727504114
PTEN
0.790 0.160 10 87952261 splice donor variant T/C;G snv 8
rs786203847
PTEN
0.790 0.160 10 87925512 splice acceptor variant G/A;C snv 8
rs121909221
PTEN
0.790 0.160 10 87952135 missense variant T/A snv 7
rs121909226
PTEN
0.790 0.160 10 87925557 missense variant T/C snv 7
rs121909228
PTEN
0.790 0.160 10 87957984 stop gained G/T snv 7
rs1554825165
PTEN
0.790 0.160 10 87957872 stop gained C/A snv 7
rs1554825530
PTEN
0.790 0.160 10 87960957 frameshift variant -/CT;TTCT ins 7
rs1554825643
PTEN
0.790 0.160 10 87961107 frameshift variant C/- delins 7
rs1554897854
PTEN
0.790 0.160 10 87931042 splice acceptor variant AGTT/- delins 7