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: rs1057517665
rs1057517665
CHAT ; SLC18A3
1 1.000 10 49611297 missense variant G/C snv 0.800 0
dbSNP: rs1057517666
rs1057517666
CHAT ; SLC18A3
1 1.000 10 49611932 missense variant G/C snv 0.800 0