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: rs1036477
rs1036477
4 0.846 0.036 15 48622729 intron variant A/G snp 0.23 0.010 1.000 1 2015 2015
dbSNP: rs10519177
rs10519177
2 0.923 0.036 15 48464998 intron variant A/G snp 0.35 0.010 1.000 1 2015 2015
dbSNP: rs140598
rs140598
5 0.821 0.143 15 48487333 missense variant G/A,C snp 3.2E-02 1.8E-02 0.010 1.000 1 1997 1997
dbSNP: rs191645600
rs191645600
1 1.000 0.036 9 136505728 missense variant G/T snp 5.8E-04 3.8E-04 0.010 1.000 1 2007 2007
dbSNP: rs2043211
rs2043211
13 0.734 0.214 19 48234449 missense variant A/T snp 0.33 0.31 0.010 1.000 1 2012 2012
dbSNP: rs2118181
rs2118181
5 0.846 0.036 15 48623687 intron variant T/C snp 0.22 0.010 1.000 1 2015 2015
dbSNP: rs4774517
rs4774517
3 0.878 0.036 15 48467094 intron variant G/T snp 0.34 0.010 1.000 1 2015 2015
dbSNP: rs755251
rs755251
2 0.923 0.036 15 48519823 intron variant A/G,T snp 0.35 0.010 1.000 1 2015 2015
dbSNP: rs761508282
rs761508282
3 0.878 0.071 9 136508288 G/C snp 8.1E-06 3.2E-05 0.010 1.000 1 2013 2013