Source: CLINVAR ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519927
PIK3CA
0.716 0.240 3 179218295 missense variant A/C;G;T snv 18
rs866775781
TP53
0.716 0.440 17 7675216 splice acceptor variant C/A;G snv 17
rs1057519942
PIK3CA
0.724 0.320 3 179203760 missense variant G/A snv 15
rs1057519895
FBXW7
0.724 0.240 4 152328232 missense variant C/A;G;T snv 14
rs397517201
PIK3CA
0.732 0.240 3 179218307 missense variant A/C;G;T snv 14
rs867384286
FBXW7
0.732 0.240 4 152328233 missense variant G/A;C snv 4.3E-06 14
rs587777790
PIK3CA
0.732 0.280 3 179199690 missense variant G/A snv 12
rs121913396
CTNNB1
0.732 0.200 3 41224607 missense variant A/C;G;T snv 11
rs587780071
TP53
0.732 0.240 17 7674951 missense variant G/A snv 11
rs377767347
SMAD4
0.742 0.520 18 51065549 missense variant G/A;C;T snv 13
rs1057519896
FBXW7
0.742 0.320 4 152326136 missense variant C/A;T snv 12
rs149680468
FBXW7
0.742 0.320 4 152326137 missense variant G/A;C;T snv 12
rs398124146
CREBBP
0.742 0.360 16 3738617 missense variant G/A;C snv 12
rs121913228
CTNNB1
0.742 0.200 3 41224621 missense variant T/C;G snv 11
rs1057519940
PIK3CA
0.752 0.200 3 179218308 missense variant G/T snv 13
rs747241612
FBXW7
0.752 0.240 4 152326215 missense variant G/C snv 4.0E-06 12
rs866987936
FBXW7
0.752 0.240 4 152326214 missense variant C/A;G;T snv 12
rs1057519884
CREBBP
0.752 0.240 16 3738616 missense variant C/A;T snv 11
rs1057519816
ERBB2
0.763 0.200 17 39711955 missense variant C/A;T snv 10
rs1057519921
NFE2L2
0.763 0.240 2 177234231 missense variant T/C snv 7
rs80338963
SMAD4
0.776 0.280 18 51065548 missense variant C/A;G;T snv 11
rs1057519929
PIK3CA
0.776 0.320 3 179199066 missense variant G/A snv 9
rs1057519941
PIK3CA
0.776 0.240 3 179203761 missense variant T/C;G snv 9
rs587777894
MTOR
0.776 0.240 1 11124516 missense variant G/A;T snv 9
rs104894231
LRRC56 ; HRAS
0.776 0.360 11 533467 missense variant C/G;T snv 7