Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519929
PIK3CA
0.776 0.320 3 179199066 missense variant G/A snv 10
rs1057519938
PIK3CA
0.776 0.160 3 179203764 missense variant A/C;T snv 10
rs1057519939
PIK3CA
0.776 0.160 3 179203763 missense variant A/C snv 10
rs1057519941
PIK3CA
0.776 0.240 3 179203761 missense variant T/C;G snv 10
rs867262025
PIK3CA
0.790 0.360 3 179221146 missense variant G/A snv 10
rs1057519928
PIK3CA
0.807 0.200 3 179221147 missense variant A/C snv 8
rs17849071
PIK3CA
0.776 0.160 3 179218439 intron variant T/G snv 7.9E-02 8
rs6443624
PIK3CA
0.776 0.200 3 179179886 intron variant C/A snv 0.30 8
rs749415085
PIK3CA
0.807 0.160 3 179198937 missense variant C/A;G;T snv 7
rs772110575
PIK3CA
0.807 0.160 3 179198938 missense variant G/A;T snv 4.0E-06 7
rs1057519931
PIK3CA
0.827 0.160 3 179199141 missense variant G/C snv 6
rs863225460
PIK3CA
0.882 0.200 3 179199160 missense variant T/A snv 5
rs121913277
PIK3CA
0.925 0.280 3 179234302 missense variant G/A;C snv 4
rs121913282
PIK3CA
0.882 0.040 3 179221072 missense variant A/C snv 4
rs397517202
PIK3CA
0.851 0.320 3 179234230 missense variant A/G snv 4
rs7646409
PIK3CA
0.882 0.040 3 179182405 intron variant T/C snv 0.26 4
rs6443626
PIK3CA ; KCNMB3
0.851 0.200 3 179237995 3 prime UTR variant T/C snv 0.24 4
rs1064793732
PIK3CA
0.882 0.320 3 179204536 missense variant G/A snv 3
rs17849079
PIK3CA
0.882 0.120 3 179234232 synonymous variant C/T snv 2.1E-02 1.5E-02 3
rs3729693
PIK3CA
3 179230408 intron variant A/G snv 1.0E-02 4.1E-02 3
rs397514565
PIK3CA
0.882 0.240 3 179204576 missense variant G/A snv 3
rs9866361
PIK3CA
0.882 0.040 3 179190061 intron variant G/A snv 0.24 3
rs3976507
PIK3CA ; KCNMB3
0.882 0.120 3 179239995 3 prime UTR variant C/T snv 0.19 0.24 3
rs1057519699
PIK3CA
3 179218315 missense variant G/A snv 2
rs121913288
PIK3CA
1.000 0.200 3 179234219 missense variant A/G snv 2