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: rs397514644
rs397514644
AKT1
2 0.925 0.040 14 104780190 missense variant G/A snv 7.0E-06 0.800 1.000 1 2013 2013
dbSNP: rs397514645
rs397514645
AKT1
1 1.000 14 104770805 missense variant T/G snv 0.800 1.000 1 2013 2013