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: rs35300242
rs35300242
5 0.827 0.120 2 233260144 intron variant G/A;C snv 0.700 1.000 1 2016 2016
dbSNP: rs36001488
rs36001488
14 0.724 0.240 2 233276621 intron variant C/T snv 0.44 0.700 1.000 1 2015 2015