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: rs9272346
rs9272346
8 0.790 0.320 6 32636595 intron variant G/A snv 0.54 0.810 1.000 3 2007 2015
dbSNP: rs17211510
rs17211510
2 1.000 0.120 6 32634653 intron variant C/A snv 0.26 0.700 1.000 1 2007 2007
dbSNP: rs2187668
rs2187668
20 0.701 0.480 6 32638107 intron variant C/T snv 3.3E-03 0.700 1.000 1 2007 2007
dbSNP: rs7990
rs7990
1 1.000 0.120 6 32642188 missense variant C/A snv 6.6E-02 1.3E-02 0.010 < 0.001 1 2013 2013