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: rs1267969615
rs1267969615
ACE
100 0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 0.020 1.000 2 2007 2011
dbSNP: rs770016471
rs770016471
ACE
1 1.000 0.040 17 63497260 missense variant C/G snv 1.4E-05 0.010 1.000 1 2011 2011