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: rs12191655
rs12191655
4 0.925 0.120 6 25802867 intron variant G/T snv 0.14 0.700 1.000 1 2009 2009
dbSNP: rs12200962
rs12200962
4 0.925 0.120 6 25828758 intron variant T/C snv 0.17 0.700 1.000 1 2009 2009
dbSNP: rs12211184
rs12211184
4 0.925 0.120 6 25823546 intron variant G/A snv 0.17 0.700 1.000 1 2009 2009
dbSNP: rs12215823
rs12215823
4 0.925 0.120 6 25725846 upstream gene variant G/C;T snv 0.700 1.000 1 2009 2009
dbSNP: rs17342717
rs17342717
6 6 25821542 intron variant C/T snv 6.1E-02 0.700 1.000 1 2009 2009
dbSNP: rs6923367
rs6923367
4 0.925 0.120 6 25745624 intergenic variant A/T snv 0.26 0.700 1.000 1 2009 2009