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: rs776280797
rs776280797
ATP7B
1 1.000 0.160 13 51939104 missense variant C/T snv 8.4E-05 5.6E-05 0.810 1.000 34 1995 2017