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: rs587777004
rs587777004
3 1.000 0.080 1 244842055 missense variant A/C;G snv 4.0E-06 0.800 1.000 3 2013 2018