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: rs10524523
rs10524523
7 0.784 0.179 19 44899792 intron variant CTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT/C. microsatellite 0.010 1.000 1 2016 2016
dbSNP: rs1157659
rs1157659
1 1.000 0.036 11 27736075 intron variant A/G snp 0.39 0.010 1.000 1 2014 2014
dbSNP: rs1187120
rs1187120
2 0.923 0.036 6 34182850 regulatory region variant T/C snp 0.99 0.010 1.000 1 2016 2016
dbSNP: rs1557372
rs1557372
1 1.000 0.036 21 41460614 regulatory region variant C/T snp 0.39 0.010 1.000 1 2013 2013
dbSNP: rs1800764
rs1800764
8 0.801 0.250 17 63473168 intergenic variant C/G,T snp 0.45 0.010 1.000 1 2015 2015
dbSNP: rs2344484
rs2344484
3 0.923 0.036 5 135540941 intergenic variant A/G snp 0.45 0.010 1.000 1 2009 2009
dbSNP: rs2731880
rs2731880
2 0.923 0.036 5 36603282 intergenic variant T/C snp 0.53 0.010 1.000 1 2015 2015
dbSNP: rs3851179
rs3851179
8 0.769 0.214 11 86157598 intergenic variant T/C snp 0.69 0.010 1.000 1 2017 2017
dbSNP: rs9877502
rs9877502
2 0.923 0.071 3 190951729 intergenic variant G/A snp 0.40 0.010 1.000 1 2013 2013
dbSNP: rs4291
rs4291
ACE
13 0.784 0.107 17 63476833 regulatory region variant T/A,C snp 0.64 0.010 1.000 1 2015 2015
dbSNP: rs1229984
rs1229984
50 0.622 0.393 4 99318162 missense variant T/C,G snp 0.90 0.94 0.010 < 0.001 1 2014 2014
dbSNP: rs1938526
rs1938526
2 0.923 0.036 10 60540625 intron variant A/G snp 9.4E-02 0.010 1.000 1 2015 2015
dbSNP: rs13133980
rs13133980
1 1.000 0.036 4 41000929 intron variant G/A,C,T snp 0.49 0.010 1.000 1 2013 2013
dbSNP: rs267606663
rs267606663
1 1.000 0.036 19 44909021 missense variant G/A,C snp 7.3E-06 3.2E-05 0.010 1.000 1 2012 2012
dbSNP: rs769449
rs769449
7 0.878 0.107 19 44906745 non coding transcript exon variant G/A snp 9.1E-02 0.010 1.000 1 2014 2014
dbSNP: rs371425292
rs371425292
APP
8 0.821 0.107 21 25897627 missense variant C/T snp 8.0E-06 0.020 1.000 2 2005 2012
dbSNP: rs572842823
rs572842823
APP
9 0.821 0.107 21 25897626 missense variant T/A snp 0.020 1.000 2 2005 2012
dbSNP: rs63750847
rs63750847
APP
6 0.801 0.143 21 25897620 missense variant C/T snp 4.5E-04 7.6E-04 0.020 1.000 2 2012 2014
dbSNP: rs193922916
rs193922916
APP
6 0.821 0.071 21 25897619 missense variant G/A snp 0.010 1.000 1 2013 2013
dbSNP: rs202074408
rs202074408
APP
8 0.801 0.143 21 26000152 missense variant G/A snp 1.6E-05 0.010 1.000 1 2016 2016
dbSNP: rs34725003
rs34725003
APP
8 0.801 0.143 21 25982424 frameshift variant GG/G in-del 0.010 1.000 1 2016 2016
dbSNP: rs369990738
rs369990738
APP
8 0.801 0.143 21 25975074 missense variant G/A snp 1.2E-05 0.010 1.000 1 2016 2016
dbSNP: rs781049584
rs781049584
APP
12 0.784 0.214 21 26021917 missense variant T/G snp 8.2E-06 0.010 1.000 1 2014 2014
dbSNP: rs165599
rs165599
18 0.715 0.250 22 19969258 3 prime UTR variant G/A snp 0.57 0.010 1.000 1 2012 2012
dbSNP: rs12273363
rs12273363
6 0.846 0.071 11 27723312 intron variant T/C snp 0.16; 3.2E-05 0.010 1.000 1 2012 2012