Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057517809
PTEN
0.882 0.160 10 87965286 splice acceptor variant G/A;C snv 4
rs1060500122
PTEN
1.000 0.080 10 87933204 stop gained C/T snv 2
rs1060500126
PTEN
0.790 0.160 10 87933223 missense variant A/C;G snv 8
rs1064793243
PTEN
1.000 0.080 10 87933082 missense variant T/C snv 2
rs1064793345
PTEN
0.752 0.240 10 87961039 missense variant T/C snv 11
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
rs1085308048
PTEN
0.851 0.320 10 87933175 stop gained T/G snv 6
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
rs1114167624
PTEN
1.000 0.080 10 87961120 splice donor variant T/C;G snv 2
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
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
rs121909221
PTEN
0.790 0.160 10 87952135 missense variant T/A snv 7
rs121909222
PTEN
0.742 0.240 10 87933127 missense variant A/G snv 13
rs121909223
PTEN
0.790 0.160 10 87933129 missense variant T/C;G snv 8
rs121909224
PTEN
0.627 0.560 10 87933147 stop gained C/G;T snv 1.2E-05 41
rs121909225
PTEN
0.790 0.160 10 87894049 missense variant T/C;G snv 8
rs121909226
PTEN
0.790 0.160 10 87925557 missense variant T/C snv 7
rs121909227
PTEN
0.776 0.240 10 87957858 stop gained C/T snv 8
rs121909228
PTEN
0.790 0.160 10 87957984 stop gained G/T snv 7
rs121909229
PTEN
0.683 0.400 10 87933148 missense variant G/A;C;T snv 23
rs121909230
PTEN
0.925 0.080 10 87933094 missense variant T/C snv 2