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: rs11122577
rs11122577
AGT
2 1.000 0.120 1 230711810 intron variant C/A snv 0.19 0.010 1.000 1 2016 2016
dbSNP: rs121918043
rs121918043
2 0.925 0.120 4 88046854 missense variant A/T snv 0.010 1.000 1 2016 2016
dbSNP: rs1222213359
rs1222213359
62 0.574 0.720 6 43770966 missense variant G/A snv 0.010 1.000 1 2008 2008
dbSNP: rs1249050389
rs1249050389
2 0.925 0.240 9 95485696 stop gained G/C snv 0.010 1.000 1 2018 2018
dbSNP: rs1392093609
rs1392093609
1 1.000 0.120 4 88007759 missense variant C/T snv 0.010 < 0.001 1 2003 2003
dbSNP: rs1464816
rs1464816
REN
2 1.000 0.120 1 204159726 intron variant T/C;G snv 0.010 1.000 1 2016 2016
dbSNP: rs1487813753
rs1487813753
1 1.000 0.120 10 100293336 missense variant T/C;G snv 8.0E-06 0.010 < 0.001 1 2017 2017
dbSNP: rs1800470
rs1800470
107 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.010 < 0.001 1 2003 2003
dbSNP: rs4362
rs4362
ACE
9 0.807 0.240 17 63496400 missense variant T/C;G snv 0.52; 1.2E-05 0.51 0.010 1.000 1 2016 2016
dbSNP: rs4762
rs4762
AGT
35 0.637 0.440 1 230710231 missense variant G/A snv 0.12 0.11 0.010 1.000 1 2016 2016
dbSNP: rs5370
rs5370
37 0.630 0.520 6 12296022 missense variant G/T snv 0.23 0.21 0.010 1.000 1 2006 2006
dbSNP: rs58598099
rs58598099
3 0.882 0.200 16 2116917 missense variant A/G snv 0.010 1.000 1 2006 2006
dbSNP: rs746231889
rs746231889
1 1.000 0.120 19 11447152 missense variant C/A;G;T snv 4.0E-06; 1.9E-04 0.010 < 0.001 1 2005 2005
dbSNP: rs754868200
rs754868200
2 0.925 0.200 4 88052022 missense variant A/G snv 1.6E-05 7.0E-06 0.010 1.000 1 2012 2012
dbSNP: rs778235410
rs778235410
2 0.925 0.120 4 88067946 stop gained C/G;T snv 2.4E-05; 1.2E-05 0.010 1.000 1 2017 2017
dbSNP: rs886041114
rs886041114
2 1.000 0.120 4 88046642 missense variant G/A;T snv 4.0E-06 0.010 1.000 1 2011 2011
dbSNP: rs1267969615
rs1267969615
ACE
100 0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 0.020 1.000 2 1997 2000
dbSNP: rs4961
rs4961
27 0.683 0.400 4 2904980 missense variant G/A;T snv 1.2E-05; 0.20 0.020 1.000 2 2003 2003
dbSNP: rs699
rs699
AGT
134 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.030 1.000 3 1997 2003
dbSNP: rs1799983
rs1799983
246 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.060 1.000 6 2002 2014
dbSNP: rs1553925453
rs1553925453
2 0.925 0.120 4 88038371 missense variant C/T snv 0.700 1.000 9 2002 2017
dbSNP: rs749004212
rs749004212
1 1.000 0.120 4 88038365 stop gained C/T snv 4.0E-06 1.4E-05 0.700 1.000 7 1999 2016
dbSNP: rs1131692280
rs1131692280
3 0.925 0.120 4 88043458 splice donor variant G/A snv 8.0E-06 1.4E-05 0.700 1.000 5 2000 2012
dbSNP: rs121918040
rs121918040
2 0.925 0.120 4 88065479 stop gained C/T snv 7.0E-06 0.700 1.000 4 1996 2013
dbSNP: rs1187336837
rs1187336837
1 1.000 0.120 4 88007931 frameshift variant C/-;CC delins 0.700 1.000 3 1999 2012