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: rs1008459
rs1008459
1 1.000 0.080 1 175182047 intron variant T/C snv 0.25 0.700 1.000 1 2007 2007