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: rs2269060
rs2269060
1 1.000 0.120 9 120921291 intron variant C/T snv 0.52 0.800 1.000 1 2012 2012