rs746485916, ATP7B

N. diseases: 1
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Hepatolenticular Degeneration
CUI: C0019202
Disease: Hepatolenticular Degeneration
349 1.000 0.160 13 51944231 missense variant G/A;C snv 3.2E-05; 4.0E-06 0.810 1.000 34 1995 2017