rs201038679, 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 51946369 missense variant G/A;T snv 3.6E-05 1.4E-05 0.820 1.000 37 1995 2017