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: rs879253743
rs879253743
1 1.000 0.036 2 100975538 missense variant C/A,G snp 0.700 1 2015 2015
dbSNP: rs10842262
rs10842262
2 0.923 0.036 12 24031610 intron variant G/C snp 0.44 0.020 0.500 2 2012 2015
dbSNP: rs12097821
rs12097821
2 0.923 0.036 1 106793679 G/A,T snp 3.2E-05; 0.19 0.020 0.500 2 2012 2015
dbSNP: rs2477686
rs2477686
2 0.923 0.036 1 2461209 intron variant G/C snp 0.64 0.020 1.000 2 2012 2015
dbSNP: rs11754464
rs11754464
1 1.000 0.036 6 31755958 intron variant C/T snp 3.1E-03 0.010 1.000 1 2016 2016
dbSNP: rs1406714
rs1406714
1 1.000 0.036 15 92918141 intron variant C/G,T snp 0.57 0.010 1.000 1 2014 2014
dbSNP: rs200847762
rs200847762
4 0.846 0.107 6 32129371 missense variant G/A snp 2.7E-04 3.2E-05 0.010 1.000 1 2016 2016
dbSNP: rs2126986
rs2126986
1 1.000 0.036 16 56317795 intron variant A/G snp 0.49 0.010 1.000 1 2014 2014
dbSNP: rs2298090
rs2298090
1 1.000 0.036 6 26156845 missense variant A/G snp 7.7E-03 6.6E-03 0.010 1.000 1 2016 2016
dbSNP: rs3088232
rs3088232
1 1.000 0.036 1 91979700 missense variant C/G,T snp 0.21; 1.6E-05 0.18; 3.2E-05 0.010 < 0.001 1 2015 2015
dbSNP: rs3129878
rs3129878
3 0.878 0.143 6 32440958 intron variant A/C snp 0.30 0.010 < 0.001 1 2015 2015
dbSNP: rs6836703
rs6836703
1 1.000 0.036 4 76108994 intron variant G/A snp 0.18 0.010 1.000 1 2008 2008
dbSNP: rs7226979
rs7226979
1 1.000 0.036 18 63257737 intron variant C/T snp 0.42 0.010 1.000 1 2014 2014