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: rs59443585
rs59443585
NEFL ; MIR6841
2 0.925 0.080 8 24955521 missense variant T/G snv 0.800 1.000 7 2000 2015