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 0.100 0.846 13 1994 2014
dbSNP: rs1415088003
rs1415088003
ACE
7 0.827 0.160 17 63489038 synonymous variant C/T snv 4.0E-06 0.040 1.000 4 1999 2007
dbSNP: rs12720742
rs12720742
ACE
1 1.000 0.040 17 63496923 missense variant C/G;T snv 2.4E-05; 3.2E-04 0.020 1.000 2 1998 2004
dbSNP: rs1221928144
rs1221928144
ACE
1 1.000 0.040 17 63477950 missense variant G/A;C snv 8.2E-06 0.010 1.000 1 2007 2007
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 1999 1999