rs770782111, 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 51946357 missense variant A/G snv 4.0E-06 0.700 1.000 20 1995 2015