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: rs756029120
rs756029120
ATP7B
1 1.000 0.160 13 51941120 missense variant C/T snv 1.2E-05 2.1E-05 0.800 1.000 35 1995 2017