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: rs14399
rs14399
3 6 111222741 3 prime UTR variant C/A snv 0.32 0.700 1.000 1 2016 2016
dbSNP: rs9400467
rs9400467
2 6 111102812 intron variant C/T snv 0.69 0.700 1.000 1 2015 2015