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: rs12704795
rs12704795
3 0.923 0.107 7 95424695 intron variant T/G snp 0.34 0.010 1.000 1 2007 2007
dbSNP: rs7582694
rs7582694
4 0.846 0.214 2 191105394 intron variant C/G snp 0.78 0.010 1.000 1 2015 2015
dbSNP: rs12026
rs12026
4 0.878 0.143 7 95411704 missense variant G/C snp 0.27 0.28 0.010 1.000 1 2007 2007
dbSNP: rs1800470
rs1800470
46 0.596 0.643 19 41353016 missense variant G/A,C snp 0.55; 2.4E-04 0.60 0.010 1.000 1 2000 2000
dbSNP: rs1800471
rs1800471
16 0.707 0.357 19 41352971 missense variant C/G,T snp 5.6E-02 6.5E-02; 3.2E-05 0.010 1.000 1 2000 2000
dbSNP: rs34557412
rs34557412
15 0.769 0.214 17 16948873 missense variant A/G snp 3.5E-03 3.3E-03 0.010 1.000 1 2006 2006
dbSNP: rs538659872
rs538659872
ACE
2 0.923 0.071 17 63496827 missense variant C/G,T snp 4.0E-06; 1.6E-05 0.010 1.000 1 2014 2014
dbSNP: rs696217
rs696217
24 0.685 0.536 3 10289773 missense variant G/T snp 8.8E-02 7.2E-02 0.010 1.000 1 2006 2006
dbSNP: rs738409
rs738409
55 0.590 0.536 22 43928847 missense variant C/G snp 0.28 0.22 0.010 1.000 1 2016 2016
dbSNP: rs7493
rs7493
23 0.679 0.357 7 95405463 missense variant G/C snp 0.27 0.28 0.010 1.000 1 2007 2007
dbSNP: rs805304
rs805304
6 0.821 0.214 6 31730311 5 prime UTR variant T/G snp 0.47 0.010 1.000 1 2013 2013
dbSNP: rs9267551
rs9267551
4 0.878 0.143 6 31730180 5 prime UTR variant C/G,T snp 0.90 0.010 1.000 1 2014 2014