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: rs864321678
rs864321678
GNMT ; CNPY3-GNMT
1 1.000 0.080 6 42962849 missense variant A/G snv 0.800 1.000 2 2002 2003
dbSNP: rs121907888
rs121907888
GNMT ; CNPY3-GNMT
1 1.000 0.080 6 42960916 missense variant T/C snv 1.8E-05 0.800 0
dbSNP: rs121907889
rs121907889
GNMT ; CNPY3-GNMT
1 1.000 0.080 6 42963149 missense variant C/A snv 4.1E-04 3.9E-04 0.800 0