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: rs1805057
rs1805057
1 1.000 0.036 6 29613344 missense variant C/T snp 1.1E-03 1.1E-03 0.020 1.000 2 2004 2006
dbSNP: rs104894718
rs104894718
7 0.801 0.143 19 35033654 missense variant C/G,T snp 4.0E-06 9.6E-05 0.010 1.000 1 2007 2007
dbSNP: rs118192250
rs118192250
4 0.878 0.107 8 132175457 missense variant C/A snp 0.010 1.000 1 2010 2010
dbSNP: rs137852779
rs137852779
2 0.923 0.036 6 52438538 missense variant A/G snp 4.0E-06 0.010 1.000 1 2007 2007
dbSNP: rs16990018
rs16990018
5 0.878 0.071 20 4699732 missense variant A/G snp 3.8E-03 1.3E-02 0.010 1.000 1 2005 2005
dbSNP: rs1799990
rs1799990
19 0.715 0.286 20 4699605 missense variant A/G snp 0.31 0.32 0.010 < 0.001 1 2008 2008
dbSNP: rs4906902
rs4906902
5 0.821 0.143 15 26774621 intron variant A/G snp 0.15 0.010 1.000 1 2012 2012
dbSNP: rs61738009
rs61738009
4 0.846 0.071 8 67483807 missense variant C/T snp 4.0E-06; 2.0E-03 2.4E-03 0.010 1.000 1 2012 2012
dbSNP: rs6295
rs6295
32 0.667 0.179 5 63962738 intron variant C/G snp 0.49 0.010 1.000 1 2013 2013
dbSNP: rs7587026
rs7587026
3 0.878 0.071 2 166122240 intron variant C/A snp 0.26 0.010 1.000 1 2013 2013
dbSNP: rs797044999
rs797044999
2 0.923 0.107 10 93797547 missense variant C/T snp 0.010 1.000 1 2010 2010