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: rs7069102
rs7069102
10 0.790 0.440 10 67903362 intron variant C/G snv 0.64 0.020 1.000 2 2008 2011
dbSNP: rs1467568
rs1467568
8 0.776 0.320 10 67915401 intron variant A/G snv 0.46 0.010 1.000 1 2009 2009
dbSNP: rs2273773
rs2273773
9 0.790 0.360 10 67906841 synonymous variant T/C snv 0.11 7.1E-02 0.010 1.000 1 2011 2011