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: rs587779004
rs587779004
1 1.000 0.080 3 37004420 missense variant A/C;G snv 0.700 1.000 20 1996 2012