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: rs1555291285
rs1555291285
ATP7B
1 1.000 0.160 13 51958537 missense variant C/G snv 0.810 1.000 25 1995 2019