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 0.909 11 1996 2009
dbSNP: rs1799752
rs1799752
ACE
25 0.677 0.480 17 63488529 intron variant -/TTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCATACAGTCACTTTT delins 0.020 1.000 2 2007 2009
dbSNP: rs1157043147
rs1157043147
ACE
1 1.000 0.120 17 63477150 missense variant T/C snv 2.8E-05 0.010 1.000 1 2003 2003
dbSNP: rs1341633213
rs1341633213
ACE
1 1.000 0.120 17 63496422 stop gained C/T snv 4.0E-06 0.010 1.000 1 2015 2015
dbSNP: rs4311
rs4311
ACE
3 0.882 0.200 17 63483402 intron variant T/C snv 0.60 0.010 1.000 1 2007 2007
dbSNP: rs4366
rs4366
ACE
1 1.000 0.120 17 63498094 3 prime UTR variant CT/-;CTCT delins 0.010 1.000 1 2007 2007