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: rs121908001
rs121908001
ATP7B
1 1.000 0.160 13 51960198 missense variant C/T snv 0.800 1.000 27 1995 2017