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 0.010 1.000 1 1999 1999
dbSNP: rs121918080
rs121918080
TTR
6 0.827 0.240 18 31595128 missense variant G/A;T snv 2.4E-05 0.010 1.000 1 2000 2000
dbSNP: rs121918090
rs121918090
TTR
8 0.790 0.240 18 31593026 missense variant G/C snv 0.010 1.000 1 2000 2000
dbSNP: rs61195471
rs61195471
6 0.827 0.160 1 156134496 missense variant G/A snv 0.010 1.000 1 2001 2001
dbSNP: rs111033560
rs111033560
9 0.807 0.040 6 118559037 stop gained T/G snv 1.6E-05 0.010 1.000 1 2003 2003
dbSNP: rs61661343
rs61661343
4 0.851 0.040 1 156130687 missense variant T/C snv 0.010 1.000 1 2004 2004
dbSNP: rs1303946678
rs1303946678
3 0.925 0.040 22 42126851 missense variant C/G snv 0.010 1.000 1 2005 2005
dbSNP: rs57045855
rs57045855
6 0.882 0.040 1 156134464 missense variant A/G;T snv 0.010 1.000 1 2006 2006
dbSNP: rs899115126
rs899115126
3 0.882 0.080 4 147542603 missense variant G/C snv 0.010 1.000 1 2006 2006
dbSNP: rs10501920
rs10501920
3 0.882 0.080 11 99622442 intron variant C/G snv 0.14 0.010 1.000 1 2007 2007
dbSNP: rs2549513
rs2549513
MAF
4 0.851 0.080 16 79516830 downstream gene variant C/A;T snv 0.010 1.000 1 2007 2007
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 2007 2007
dbSNP: rs499818
rs499818
4 0.851 0.080 6 13332235 upstream gene variant G/A snv 0.21 0.010 1.000 1 2007 2007
dbSNP: rs740363
rs740363
5 0.851 0.080 10 116816095 intron variant G/A snv 0.40 0.010 1.000 1 2007 2007
dbSNP: rs958546
rs958546
3 0.882 0.040 13 46259582 intron variant G/C snv 0.29 0.010 1.000 1 2007 2007
dbSNP: rs34376731
rs34376731
2 0.925 0.040 12 54581014 missense variant C/T snv 4.6E-03 1.9E-02 0.020 1.000 2 2008 2009
dbSNP: rs10757274
rs10757274
22 0.701 0.320 9 22096056 intron variant A/G snv 0.41 0.010 1.000 1 2009 2009
dbSNP: rs1137101
rs1137101
77 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 0.010 1.000 1 2009 2009
dbSNP: rs2383206
rs2383206
17 0.742 0.320 9 22115027 intron variant A/G snv 0.49 0.010 1.000 1 2009 2009
dbSNP: rs397516089
rs397516089
6 0.827 0.080 14 23429807 missense variant C/G;T snv 0.010 1.000 1 2009 2009
dbSNP: rs5219
rs5219
25 0.701 0.360 11 17388025 stop gained T/A;C snv 0.64 0.010 1.000 1 2009 2009
dbSNP: rs5370
rs5370
37 0.630 0.520 6 12296022 missense variant G/T snv 0.23 0.21 0.010 1.000 1 2009 2009
dbSNP: rs1800888
rs1800888
23 0.695 0.400 5 148827322 missense variant C/T snv 9.1E-03 9.1E-03 0.020 1.000 2 2009 2010
dbSNP: rs10519210
rs10519210
1 1.000 0.040 15 63445726 intergenic variant T/C;G snv 0.800 1.000 1 2010 2010
dbSNP: rs11172782
rs11172782
1 1.000 0.040 12 58865846 intergenic variant A/G snv 0.12 0.800 1.000 1 2010 2010