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: rs1800562
rs1800562
262 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 0.010 1.000 1 2009 2009
dbSNP: rs4986790
rs4986790
223 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 0.020 1.000 2 2009 2011
dbSNP: rs1799945
rs1799945
226 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 0.010 1.000 1 2009 2009
dbSNP: rs4986791
rs4986791
182 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 0.010 1.000 1 2011 2011
dbSNP: rs699
rs699
AGT
134 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.010 1.000 1 2015 2015
dbSNP: rs3025039
rs3025039
62 0.576 0.720 6 43784799 3 prime UTR variant C/T snv 0.13 0.010 1.000 1 2019 2019
dbSNP: rs4994
rs4994
65 0.578 0.640 8 37966280 missense variant A/G snv 0.11 9.2E-02 0.010 1.000 1 2008 2008
dbSNP: rs5361
rs5361
47 0.623 0.720 1 169731919 missense variant T/G snv 8.3E-02; 8.0E-06 7.8E-02 0.010 1.000 1 2007 2007
dbSNP: rs1137100
rs1137100
39 0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25 0.010 1.000 1 2014 2014
dbSNP: rs1458766475
rs1458766475
41 0.637 0.680 1 169732649 missense variant C/G;T snv 4.0E-06; 4.0E-06 0.010 1.000 1 2007 2007
dbSNP: rs1800206
rs1800206
35 0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 0.010 1.000 1 2004 2004
dbSNP: rs225014
rs225014
22 0.695 0.400 14 80203237 missense variant T/C snv 0.41 0.39 0.010 1.000 1 2010 2010
dbSNP: rs13266634
rs13266634
23 0.724 0.480 8 117172544 missense variant C/A;T snv 0.29 0.010 1.000 1 2017 2017
dbSNP: rs750359414
rs750359414
5 0.851 0.240 19 7669884 missense variant C/G;T snv 4.0E-06; 4.0E-06 0.010 1.000 1 2005 2005
dbSNP: rs16995309
rs16995309
4 0.882 0.280 20 50581336 missense variant C/T snv 4.8E-03 5.0E-03 0.010 < 0.001 1 2005 2005
dbSNP: rs45539933
rs45539933
5 0.882 0.280 4 140567914 missense variant C/T snv 8.7E-02 7.7E-02 0.010 1.000 1 2012 2012
dbSNP: rs622342
rs622342
4 0.882 0.280 6 160151834 intron variant C/A snv 0.70 0.010 1.000 1 2013 2013
dbSNP: rs1466929132
rs1466929132
3 0.925 0.200 12 21378325 missense variant G/A;C snv 4.0E-06 0.010 1.000 1 2007 2007
dbSNP: rs374057152
rs374057152
3 0.925 0.200 6 43777592 missense variant T/C snv 4.0E-06 1.4E-05 0.010 1.000 1 2015 2015
dbSNP: rs1303471186
rs1303471186
1 1.000 0.120 17 63972627 missense variant G/A;T snv 2.5E-05; 4.2E-06 0.010 1.000 1 2015 2015
dbSNP: rs1871922
rs1871922
1 1.000 0.120 3 129183756 intron variant G/C;T snv 0.010 1.000 1 2011 2011