Source: ALL
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: rs9991278
rs9991278
SLC2A9 ; LOC105374476
3 0.925 0.120 4 10001041 intron variant T/A;C snv 0.700 1.000 1 2009 2009