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: rs1217691063
rs1217691063
614 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 0.100 0.938 32 1999 2019
dbSNP: rs699
rs699
AGT
134 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.100 0.933 15 1997 2017
dbSNP: rs397507444
rs397507444
306 0.405 0.880 1 11794407 missense variant T/G snv 0.090 0.889 9 2000 2017
dbSNP: rs340874
rs340874
7 0.882 0.080 1 213985913 non coding transcript exon variant T/C snv 0.40 0.830 1.000 8 2010 2019
dbSNP: rs10923931
rs10923931
3 0.925 0.120 1 119975336 intron variant G/T snv 0.17 0.820 1.000 7 2007 2017
dbSNP: rs1800896
rs1800896
113 0.507 0.800 1 206773552 intron variant T/C snv 0.41 0.050 1.000 5 2010 2019
dbSNP: rs1801133
rs1801133
174 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 0.050 0.800 5 2012 2019
dbSNP: rs10911021
rs10911021
11 0.807 0.160 1 182112825 intron variant C/T snv 0.36 0.730 1.000 4 2013 2016
dbSNP: rs1137100
rs1137100
39 0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25 0.040 0.750 4 2005 2019
dbSNP: rs1137101
rs1137101
77 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 0.040 0.750 4 2005 2018
dbSNP: rs17106184
rs17106184
3 0.925 0.080 1 50444313 intron variant G/A snv 8.5E-02 0.820 1.000 4 2014 2017
dbSNP: rs198389
rs198389
10 0.776 0.240 1 11859214 upstream gene variant A/G snv 0.39 0.040 0.750 4 2009 2015
dbSNP: rs2228145
rs2228145
57 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 0.040 1.000 4 2004 2019
dbSNP: rs2476601
rs2476601
121 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 0.730 1.000 4 2008 2018
dbSNP: rs3737787
rs3737787
11 0.763 0.280 1 161039733 3 prime UTR variant G/A snv 0.21 0.040 1.000 4 2005 2008
dbSNP: rs4641
rs4641
6 0.851 0.120 1 156137743 splice region variant C/T snv 0.26 0.21 0.040 0.750 4 2007 2010
dbSNP: rs4762
rs4762
AGT
35 0.637 0.440 1 230710231 missense variant G/A snv 0.12 0.11 0.040 0.750 4 1997 2017
dbSNP: rs1136410
rs1136410
70 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 0.030 1.000 3 2012 2016
dbSNP: rs12742393
rs12742393
2 0.925 0.120 1 162254796 intron variant A/C;T snv 0.030 1.000 3 2010 2019
dbSNP: rs1800872
rs1800872
119 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 0.030 1.000 3 2010 2014
dbSNP: rs2274907
rs2274907
5 0.851 0.200 1 160882036 missense variant A/G;T snv 0.66 0.030 1.000 3 2007 2019
dbSNP: rs841853
rs841853
4 0.882 0.200 1 42935767 intron variant A/C snv 0.66 0.030 1.000 3 2013 2019
dbSNP: rs945508
rs945508
3 1.000 0.080 1 156937289 missense variant T/C snv 0.64 0.66 0.030 1.000 3 2007 2011
dbSNP: rs10494366
rs10494366
7 0.851 0.200 1 162115895 intron variant G/T snv 0.54 0.020 1.000 2 2010 2010
dbSNP: rs10754558
rs10754558
20 0.695 0.480 1 247448734 3 prime UTR variant G/C;T snv 0.020 1.000 2 2013 2015