Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2699887
PIK3CA ; LOC101928739
0.763 0.280 3 179148620 intron variant C/T snv 0.18 11
rs7621329
PIK3CA
1.000 0.040 3 179157086 intron variant C/T snv 0.26 1
rs4855094
PIK3CA
1.000 0.040 3 179160189 intron variant G/A snv 0.10 1
rs9838411
PIK3CA
0.925 0.080 3 179169899 intron variant G/A snv 0.25 2
rs6443624
PIK3CA
0.776 0.200 3 179179886 intron variant C/A snv 0.30 8
rs7646409
PIK3CA
0.882 0.040 3 179182405 intron variant T/C snv 0.26 4
rs7640662
PIK3CA
1.000 0.040 3 179184213 intron variant C/G snv 0.10 1
rs9866361
PIK3CA
0.882 0.040 3 179190061 intron variant G/A snv 0.24 3
rs71310379
PIK3CA
3 179199003 missense variant C/A snv 4.4E-05 4.2E-05 1
rs778184105
PIK3CA
3 179199098 missense variant C/A snv 4.1E-06 2
rs863225060
PIK3CA
0.925 0.120 3 179199136 missense variant C/T snv 1
rs863225460
PIK3CA
0.882 0.200 3 179199160 missense variant T/A snv 2
rs587777790
PIK3CA
0.732 0.280 3 179199690 missense variant G/A snv 2
rs767439253
PIK3CA
1.000 0.120 3 179199885 missense variant A/G snv 1.1E-04 1.4E-05 1
rs1260908401
PIK3CA
1.000 3 179203565 missense variant C/T snv 4.0E-06 1
rs1442481831
PIK3CA
0.925 0.080 3 179203635 missense variant T/C snv 2
rs1057519942
PIK3CA
0.724 0.320 3 179203760 missense variant G/A snv 1
rs1057519941
PIK3CA
0.776 0.240 3 179203761 missense variant T/C;G snv 1
rs121913284
PIK3CA
0.776 0.160 3 179203765 missense variant T/A;G snv 1
rs3729679
PIK3CA
1.000 0.080 3 179204642 intron variant A/G snv 0.58 1
rs2677764
PIK3CA
0.925 0.080 3 179206019 intron variant C/A;T snv 2
rs121913272
PIK3CA
0.752 0.400 3 179210192 missense variant T/C;G snv 1
rs1057519925
PIK3CA
0.683 0.560 3 179210291 missense variant G/A;C snv 1
rs12494623
PIK3CA
1.000 0.080 3 179214763 intron variant C/G;T snv 1
rs121913273
PIK3CA
0.605 0.440 3 179218294 missense variant G/A;C snv 22