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: rs2295080
rs2295080
20 0.695 0.320 1 11262571 upstream gene variant G/C;T snv 0.020 1.000 2 2014 2016
dbSNP: rs11121704
rs11121704
3 1 11233902 intron variant C/A;T snv 0.010 1.000 1 2014 2014
dbSNP: rs2536
rs2536
11 0.776 0.240 1 11106656 3 prime UTR variant T/C snv 5.8E-02 0.010 1.000 1 2016 2016