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: rs3729548
rs3729548
2 1.000 0.080 1 42934681 intron variant C/T snv 0.32 0.010 1.000 1 2018 2018
dbSNP: rs4293393
rs4293393
8 0.827 0.200 16 20353266 intron variant A/G snv 0.20 0.010 1.000 1 2017 2017
dbSNP: rs4821480
rs4821480
9 0.807 0.160 22 36299201 intron variant G/T snv 0.78 0.010 1.000 1 2011 2011
dbSNP: rs653747
rs653747
2 15 97659878 intron variant C/T snv 0.48 0.010 1.000 1 2017 2017
dbSNP: rs6610650
rs6610650
2 1.000 0.040 X 37777261 intron variant G/A snv 0.27 0.010 1.000 1 2013 2013
dbSNP: rs6677604
rs6677604
CFH
7 0.827 0.200 1 196717788 intron variant G/A snv 0.23 0.800 1.000 1 2011 2011
dbSNP: rs702553
rs702553
6 0.882 0.160 5 60440946 intron variant A/T snv 0.37 0.010 1.000 1 2013 2013
dbSNP: rs739401
rs739401
2 11 3015094 intron variant C/T snv 0.45 0.010 1.000 1 2016 2016
dbSNP: rs741301
rs741301
3 0.925 0.160 7 36878390 intron variant C/T snv 0.59 0.010 1.000 1 2016 2016
dbSNP: rs7704116
rs7704116
2 1.000 0.080 5 134216763 intron variant C/T snv 9.9E-02 0.010 1.000 1 2011 2011
dbSNP: rs7947841
rs7947841
CAT
1 11 34470133 intron variant G/A snv 1.0E-01 0.010 1.000 1 2013 2013
dbSNP: rs841853
rs841853
4 0.882 0.200 1 42935767 intron variant A/C snv 0.66 0.010 1.000 1 2018 2018
dbSNP: rs9896208
rs9896208
ACE
1 17 63498748 intron variant T/C snv 0.57 0.010 1.000 1 2005 2005
dbSNP: rs4972593
rs4972593
3 0.925 0.200 2 173598126 intergenic variant T/A snv 0.20 0.010 1.000 1 2013 2013
dbSNP: rs9974610
rs9974610
3 1.000 0.080 21 31646056 intergenic variant A/G snv 0.13 0.010 1.000 1 2008 2008
dbSNP: rs713041
rs713041
16 0.776 0.400 19 1106616 stop gained T/A;C snv 4.2E-06; 0.58 0.010 1.000 1 2013 2013
dbSNP: rs699
rs699
AGT
134 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.100 1.000 15 1996 2014
dbSNP: rs1799983
rs1799983
246 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.100 0.909 11 2007 2015
dbSNP: rs1267969615
rs1267969615
ACE
100 0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 0.080 1.000 8 1999 2014
dbSNP: rs1217691063
rs1217691063
614 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 0.060 0.667 6 1999 2012
dbSNP: rs1799945
rs1799945
226 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 0.030 1.000 3 2001 2014
dbSNP: rs11643718
rs11643718
10 0.807 0.240 16 56899607 missense variant G/A snv 0.11 8.4E-02 0.020 1.000 2 2003 2016
dbSNP: rs140511594
rs140511594
13 0.742 0.360 2 165941111 missense variant G/A snv 1.3E-04 1.1E-04 0.020 1.000 2 2014 2017
dbSNP: rs1800562
rs1800562
262 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 0.020 1.000 2 2004 2014
dbSNP: rs1801282
rs1801282
131 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 0.020 1.000 2 2007 2012