Source: CLINVAR ×
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs104886003
rs104886003
PIK3CA
34 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 0.700 0
dbSNP: rs112445441
rs112445441
KRAS
8 0.658 0.400 12 25245347 missense variant C/A;G;T snv 0.700 0
dbSNP: rs121913279
rs121913279
PIK3CA
45 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 0.700 0
dbSNP: rs121913286
rs121913286
PIK3CA
20 0.677 0.280 3 179218306 missense variant C/A;G snv 0.700 0
dbSNP: rs28934874
rs28934874
TP53
21 0.695 0.480 17 7675161 missense variant G/A;C;T snv 0.700 0