Source: ALL
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: rs1555652216
rs1555652216
DCC
1 1.000 18 53322064 missense variant C/A snv 0.700 1.000 1 2017 2017