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: rs104886302
rs104886302
4 0.878 0.143 X 108695376 missense variant G/A snp 0.010 1.000 1 2007 2007
dbSNP: rs104886303
rs104886303
3 0.878 0.179 X 108695409 missense variant T/G snp 0.010 1.000 1 2013 2013
dbSNP: rs11739136
rs11739136
9 0.846 0.143 5 170383792 missense variant C/T snp 9.9E-02 8.1E-02 0.010 1.000 1 2011 2011
dbSNP: rs121908144
rs121908144
4 0.846 0.214 1 54999221 missense variant T/C snp 2.0E-05 0.010 1.000 1 2009 2009
dbSNP: rs151340624
rs151340624
4 0.878 0.107 X 50090846 stop gained C/T snp 0.010 < 0.001 1 1999 1999
dbSNP: rs151340626
rs151340626
4 0.846 0.179 X 50085987 missense variant C/T snp 0.010 1.000 1 1998 1998
dbSNP: rs1801282
rs1801282
77 0.543 0.679 3 12351626 missense variant C/G snp 0.11 1.0E-01 0.010 1.000 1 2008 2008
dbSNP: rs1805192
rs1805192
75 0.545 0.679 3 12379739 missense variant C/G snp 0.010 1.000 1 2008 2008
dbSNP: rs200031940
rs200031940
1 1.000 0.071 11 101504770 missense variant G/A,C snp 6.1E-05; 4.1E-06 0.010 1.000 1 2016 2016
dbSNP: rs200640958
rs200640958
1 1.000 0.071 11 101471303 synonymous variant G/A,C snp 8.0E-06; 1.6E-05 0.010 1.000 1 2016 2016
dbSNP: rs2032487
rs2032487
3 0.878 0.071 22 36299382 intron variant C/T snp 0.79 0.010 1.000 1 2010 2010
dbSNP: rs2285450
rs2285450
1 1.000 0.071 19 35851365 synonymous variant G/A snp 2.2E-02 4.2E-02 0.010 1.000 1 2016 2016
dbSNP: rs3024912
rs3024912
2 0.923 0.107 2 191028361 intron variant A/C snp 0.29 0.010 1.000 1 2013 2013
dbSNP: rs437168
rs437168
1 1.000 0.071 19 35843517 synonymous variant G/A,C snp 7.9E-02; 1.2E-05 0.16 0.010 1.000 1 2016 2016
dbSNP: rs4821480
rs4821480
9 0.801 0.143 22 36299201 intron variant G/T snp 0.79 0.010 1.000 1 2010 2010
dbSNP: rs4821481
rs4821481
1 1.000 0.071 22 36299896 intron variant C/T snp 0.79 0.010 1.000 1 2010 2010
dbSNP: rs4961
rs4961
22 0.685 0.250 4 2904980 missense variant G/A,T snp 1.2E-05; 0.20 0.17 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: rs730880377
rs730880377
2 0.923 0.107 9 123370950 missense variant C/G,T snp 4.1E-06; 4.1E-06 0.010 1.000 1 2015 2015
dbSNP: rs734553
rs734553
6 0.878 0.214 4 9921380 intron variant G/A,T snp 0.70 0.010 1.000 1 2016 2016
dbSNP: rs754919065
rs754919065
1 1.000 0.071 11 101504767 missense variant G/A snp 6.1E-05; 4.1E-06 3.2E-05 0.010 1.000 1 2016 2016
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: rs760336723
rs760336723
3 0.878 0.214 7 131506292 missense variant G/A snp 2.8E-05 3.2E-05 0.010 1.000 1 2004 2004
dbSNP: rs765676223
rs765676223
3 0.923 0.107 9 123371542 missense variant C/A,G,T snp 1.6E-05; 2.3E-04 0.010 1.000 1 2015 2015