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: rs1334067073
rs1334067073
ACE
2 0.925 0.120 17 63478025 missense variant C/G;T snv 4.2E-06 0.010 1.000 1 2002 2002
dbSNP: rs4961
rs4961
27 0.683 0.400 4 2904980 missense variant G/A;T snv 1.2E-05; 0.20 0.010 1.000 1 2002 2002
dbSNP: rs553553817
rs553553817
1 1.000 0.120 4 2882046 missense variant C/T snv 8.3E-06 0.010 1.000 1 2002 2002