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: rs12885713
rs12885713
5 0.827 0.200 14 90397013 intron variant C/A;G;T snv 0.010 1.000 1 2009 2009
dbSNP: rs5871
rs5871
2 0.925 0.200 14 90405134 3 prime UTR variant T/C snv 0.12 0.010 1.000 1 2009 2009