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: rs587777231
rs587777231
EDN1
1 1.000 6 12293978 missense variant A/G snv 0.800 1.000 1 2013 2013
dbSNP: rs587777232
rs587777232
EDN1
1 1.000 6 12292506 missense variant C/A snv 0.800 1.000 1 2013 2013