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: rs2119704
rs2119704
1 1.000 0.080 14 88021345 intron variant C/A snv 0.11 0.800 1.000 1 2011 2011