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: rs1057518775
rs1057518775
5 0.846 0.143 11 17387907 missense variant G/A,C snp 9.6E-05 0.700 0
dbSNP: rs1801483
rs1801483
7 0.846 0.107 17 81809839 missense variant G/A snp 7.4E-03 3.9E-03 0.010 1.000 1 1997 1997
dbSNP: rs11575937
rs11575937
17 0.715 0.321 1 156136985 missense variant G/A,T snp 0.030 1.000 3 2000 2001
dbSNP: rs1801282
rs1801282
77 0.543 0.679 3 12351626 missense variant C/G snp 0.11 1.0E-01 0.060 1.000 6 2001 2010
dbSNP: rs1805192
rs1805192
75 0.545 0.679 3 12379739 missense variant C/G snp 0.060 1.000 6 2001 2010
dbSNP: rs1799883
rs1799883
26 0.679 0.250 4 119320747 missense variant T/A,C,G snp 0.73 0.74 0.010 < 0.001 1 2001 2001
dbSNP: rs1799983
rs1799983
138 0.475 0.786 7 150999023 missense variant T/A,G snp 0.75 0.76 0.010 1.000 1 2002 2002
dbSNP: rs137852671
rs137852671
9 0.784 0.143 11 17394295 missense variant C/T snp 0.020 0.500 2 2003 2011
dbSNP: rs148969251
rs148969251
1 1.000 0.036 11 120480110 missense variant A/G snp 3.3E-02 8.0E-03 0.010 1.000 1 2006 2006
dbSNP: rs1016862
rs1016862
2 1.000 0.036 18 60371844 missense variant A/C snp 0.010 1.000 1 2009 2009
dbSNP: rs2918419
rs2918419
3 0.878 0.071 5 143342788 intron variant T/C snp 0.16 0.010 < 0.001 1 2009 2009
dbSNP: rs2943641
rs2943641
13 0.769 0.143 2 226229029 intergenic variant T/C snp 0.67 0.010 1.000 1 2009 2009
dbSNP: rs3732581
rs3732581
7 0.801 0.107 3 183840614 missense variant C/G,T snp 0.46; 1.2E-05 0.46 0.010 1.000 1 2009 2009
dbSNP: rs587777260
rs587777260
2 0.923 0.071 13 75359852 stop gained G/A,T snp 4.0E-06 0.010 1.000 1 2009 2009
dbSNP: rs9402571
rs9402571
4 0.878 0.071 6 134167822 intergenic variant T/G snp 0.23 0.010 1.000 1 2009 2009
dbSNP: rs225014
rs225014
13 0.734 0.321 14 80203237 missense variant T/C snp 0.41 0.37 0.010 1.000 1 2010 2010
dbSNP: rs33997857
rs33997857
1 1.000 0.036 2 11787112 missense variant G/A,T snp 1.6E-02 2.4E-02 0.010 1.000 1 2010 2010
dbSNP: rs4629571
rs4629571
2 0.923 0.143 5 75362479 intron variant A/G snp 8.7E-02 0.010 1.000 1 2010 2010
dbSNP: rs6708316
rs6708316
2 0.923 0.071 2 11797032 intron variant G/C,T snp 0.38 0.010 1.000 1 2010 2010
dbSNP: rs8192678
rs8192678
16 0.734 0.286 4 23814039 missense variant C/T snp 0.31 0.26 0.010 1.000 1 2010 2010
dbSNP: rs9997745
rs9997745
2 0.923 0.036 4 184816689 intron variant G/A snp 0.24 0.010 1.000 1 2010 2010
dbSNP: rs4986790
rs4986790
146 0.465 0.750 9 117713024 missense variant A/G,T snp 6.1E-02; 4.0E-06 6.7E-02 0.010 1.000 1 2011 2011
dbSNP: rs121913564
rs121913564
4 0.878 0.071 18 60371403 missense variant A/C snp 2.0E-05 0.010 1.000 1 2012 2012
dbSNP: rs746906443
rs746906443
3 0.923 0.071 18 60371868 missense variant A/G snp 4.0E-06 0.010 1.000 1 2012 2012
dbSNP: rs10423928
rs10423928
5 0.878 0.107 19 45679046 intron variant T/A snp 0.20 0.010 1.000 1 2013 2013