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 0.060 1.000 6 1999 2007
dbSNP: rs1799752
rs1799752
ACE
25 0.677 0.480 17 63488529 intron variant -/TTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCATACAGTCACTTTT delins 0.020 1.000 2 2009 2016
dbSNP: rs4291
rs4291
ACE
20 0.724 0.400 17 63476833 upstream gene variant T/A;C snv 0.020 1.000 2 2006 2012
dbSNP: rs1042309696
rs1042309696
ACE
2 17 63487006 synonymous variant T/C snv 0.010 1.000 1 2008 2008
dbSNP: rs1415088003
rs1415088003
ACE
7 0.827 0.160 17 63489038 synonymous variant C/T snv 4.0E-06 0.010 1.000 1 2010 2010
dbSNP: rs1455404812
rs1455404812
ACE
2 1.000 0.080 17 63488732 missense variant C/T snv 0.010 1.000 1 2016 2016
dbSNP: rs765803965
rs765803965
ACE
1 17 63480345 missense variant G/A snv 4.0E-06 0.010 1.000 1 2008 2008
dbSNP: rs779175881
rs779175881
ACE
2 1.000 0.080 17 63496959 missense variant C/T snv 2.4E-05 1.4E-05 0.010 1.000 1 2016 2016