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: rs121908991
rs121908991
PRKAG2
6 0.807 0.120 7 151560610 missense variant C/A;T snv 0.800 1.000 5 2001 2016
dbSNP: rs121908987
rs121908987
PRKAG2
12 0.742 0.200 7 151576412 missense variant C/A;G;T snv 4.0E-06 0.700 1.000 6 2004 2015
dbSNP: rs267606977
rs267606977
PRKAG2
4 0.851 0.120 7 151560613 missense variant T/C snv 0.700 1.000 3 2008 2016
dbSNP: rs730882148
rs730882148
PRKAG2
1 1.000 0.120 7 151568798 missense variant C/G snv 0.700 0