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: rs864309722
rs864309722
MECOM
1 1.000 3 169100904 missense variant T/C snv 0.800 1.000 1 2015 2015
dbSNP: rs864309723
rs864309723
MECOM
1 1.000 3 169100918 missense variant T/C snv 0.800 1.000 1 2015 2015
dbSNP: rs864309724
rs864309724
MECOM
1 1.000 3 169100922 missense variant G/A snv 0.800 1.000 1 2015 2015