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: rs897959
rs897959
1 1.000 0.080 1 243734472 intron variant C/T snv 0.50 0.010 1.000 1 2009 2009