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 0.030 0.333 3 2001 2011
dbSNP: rs568401628
rs568401628
ACE
4 0.882 0.120 17 63497280 missense variant C/T snv 4.5E-05 7.0E-06 0.010 1.000 1 2004 2004