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: rs201201843
rs201201843
PLEKHG2
2 0.925 0.160 19 39416866 missense variant C/T snv 3.6E-04 3.8E-04 0.010 1.000 1 2016 2016