Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs562015640
PTEN
0.742 0.360 10 87960957 stop gained A/G;T snv 1.2E-05 15
rs121909218
PTEN
0.672 0.360 10 87933145 missense variant G/A snv 12
rs2735343
PTEN
0.790 0.240 10 87945672 non coding transcript exon variant G/C snv 0.39 11
rs1205454520
KLLN ; PTEN
0.763 0.120 10 87864059 5 prime UTR variant -/G delins 7.2E-06 10
rs701848
PTEN
0.807 0.280 10 87966988 3 prime UTR variant T/C snv 0.33 10
rs786204929
PTEN
0.752 0.200 10 87933144 stop gained G/A;T snv 9
rs121909224
PTEN
0.627 0.560 10 87933147 stop gained C/G;T snv 1.2E-05 7
rs121909235
PTEN
0.851 0.240 10 87957919 missense variant G/A snv 7
rs1029342144
KLLN ; PTEN
0.882 0.120 10 87864162 5 prime UTR variant C/G;T snv 6
rs121909222
PTEN
0.742 0.240 10 87933127 missense variant A/G snv 6
rs765433422
PTEN
0.807 0.160 10 87952250 stop gained G/A;T snv 8.0E-06 7.0E-06 6
rs11202592
KLLN ; PTEN
0.851 0.200 10 87864461 5 prime UTR variant C/G snv 3.8E-03 1.4E-03 5
rs121909231
PTEN
0.667 0.600 10 87961095 stop gained C/A;T snv 5
rs2299939
PTEN
0.827 0.080 10 87897393 intron variant C/A;T snv 5
rs868257011
PTEN
0.925 0.080 10 87961042 frameshift variant TACTT/- del 4
rs1114167628
PTEN
0.925 0.080 10 87961033 stop gained -/ATATCTAG delins 4
rs779530981
PTEN
1.000 0.160 10 87933035 missense variant C/A snv 4
rs1197734477
PTEN
0.925 0.080 10 87961012 missense variant A/G snv 4
rs1234220
PTEN
0.851 0.080 10 87885716 intron variant A/G snv 9.1E-02 4
rs786201044
PTEN
0.827 0.200 10 87933165 missense variant T/C snv 3
rs9651492
PTEN
0.882 0.160 10 87933216 missense variant G/A;C snv 3
rs2299941
PTEN
0.882 0.080 10 87944962 intron variant A/G snv 9.7E-02 3
rs3830675
PTEN
1.000 0.040 10 87931195 intron variant -/TCTTA delins 3
rs121913294
PTEN
0.776 0.280 10 87952143 missense variant G/A;C;T snv 8.0E-06 3
rs778528056
PTEN
0.882 0.040 10 87957886 missense variant A/G;T snv 3