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: rs2861887
rs2861887
1 1.000 0.080 1 177072861 intron variant C/T snv 0.46 0.700 1.000 1 2009 2009