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: rs115336700
rs115336700
1 1.000 0.040 17 7631341 missense variant G/A;C snv 2.8E-05; 1.7E-03 0.010 1.000 1 2006 2006
dbSNP: rs6257
rs6257
5 0.827 0.200 17 7630399 3 prime UTR variant T/C snv 9.4E-02 8.1E-02 0.010 1.000 1 2013 2013
dbSNP: rs3760213
rs3760213
1 1.000 0.040 17 7629896 intron variant G/A snv 7.8E-02 0.010 1.000 1 2014 2014
dbSNP: rs6259
rs6259
27 0.658 0.400 17 7633209 missense variant G/A snv 8.9E-02 8.1E-02 0.010 1.000 1 2014 2014
dbSNP: rs1799941
rs1799941
11 0.763 0.280 17 7630105 5 prime UTR variant G/A snv 0.18 0.020 1.000 2 2013 2015