Source: ALL
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: rs1260908401
rs1260908401
PIK3CA
1 1.000 3 179203565 missense variant C/T snv 4.0E-06 0.010 1.000 1 2006 2006
dbSNP: rs867171992
rs867171992
PTEN
1 1.000 10 87960926 missense variant C/G snv 0.010 1.000 1 2006 2006