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: rs501120
rs501120
10 0.763 0.240 10 44258419 downstream gene variant T/C snv 0.24 0.020 0.500 2 2012 2013
dbSNP: rs1746048
rs1746048
8 0.776 0.120 10 44280376 downstream gene variant C/T snv 0.25 0.010 1.000 1 2013 2013
dbSNP: rs1867624
rs1867624
4 0.851 0.080 17 64309731 upstream gene variant C/T snv 0.65 0.010 1.000 1 2017 2017
dbSNP: rs1878406
rs1878406
7 0.807 0.200 4 147472512 intergenic variant C/A;G;T snv 0.010 < 0.001 1 2014 2014
dbSNP: rs2107595
rs2107595
15 0.732 0.280 7 19009765 regulatory region variant G/A snv 0.19 0.010 1.000 1 2019 2019
dbSNP: rs2943634
rs2943634
15 0.763 0.200 2 226203364 intergenic variant A/C;G snv 0.010 1.000 1 2013 2013
dbSNP: rs2943641
rs2943641
18 0.763 0.160 2 226229029 intergenic variant T/C snv 0.67 0.010 1.000 1 2013 2013
dbSNP: rs2943650
rs2943650
6 0.827 0.120 2 226241205 intergenic variant C/T snv 0.58 0.010 1.000 1 2013 2013
dbSNP: rs2972146
rs2972146
9 0.882 0.040 2 226235982 intergenic variant G/T snv 0.72 0.010 1.000 1 2013 2013
dbSNP: rs3939286
rs3939286
12 0.776 0.360 9 6210099 regulatory region variant T/A;C snv 0.010 1.000 1 2015 2015
dbSNP: rs4552883
rs4552883
2 0.925 0.040 8 139234730 regulatory region variant G/A;C snv 0.010 1.000 1 2011 2011
dbSNP: rs7833904
rs7833904
3 0.882 0.040 8 58505103 upstream gene variant A/T snv 0.55 0.010 < 0.001 1 2015 2015
dbSNP: rs8042271
rs8042271
3 0.882 0.040 15 89030987 intergenic variant G/A;T snv 0.010 1.000 1 2019 2019
dbSNP: rs974819
rs974819
6 0.807 0.080 11 103789839 intron variant T/A;C snv 0.010 1.000 1 2014 2014
dbSNP: rs2230806
rs2230806
24 0.689 0.280 9 104858586 missense variant C/T snv 0.32 0.39 0.040 0.750 4 2003 2018
dbSNP: rs2066714
rs2066714
13 0.742 0.240 9 104824472 missense variant T/C snv 0.21 0.25 0.010 1.000 1 2014 2014
dbSNP: rs2066715
rs2066715
7 0.807 0.160 9 104825752 missense variant C/T snv 8.2E-02 5.5E-02 0.010 < 0.001 1 2015 2015
dbSNP: rs28937313
rs28937313
3 0.882 0.160 9 104822520 missense variant T/C snv 8.0E-06 0.010 1.000 1 2013 2013
dbSNP: rs4149313
rs4149313
9 0.763 0.240 9 104824472 missense variant T/C snv 0.010 1.000 1 2014 2014
dbSNP: rs57137919
rs57137919
9 0.776 0.160 21 42218908 intron variant G/A snv 0.14 0.010 1.000 1 2014 2014
dbSNP: rs1267969615
rs1267969615
ACE
100 0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 0.010 1.000 1 2007 2007
dbSNP: rs4862423
rs4862423
4 0.882 0.080 4 184805394 intron variant C/T snv 0.37 0.010 1.000 1 2016 2016
dbSNP: rs3825807
rs3825807
10 0.807 0.120 15 78796769 missense variant A/G snv 0.34 0.33 0.030 1.000 3 2013 2019
dbSNP: rs6918289
rs6918289
2 0.925 0.040 6 41134089 intron variant G/T snv 9.8E-02 0.010 1.000 1 2018 2018
dbSNP: rs4961
rs4961
27 0.683 0.400 4 2904980 missense variant G/A;T snv 1.2E-05; 0.20 0.040 1.000 4 2001 2020