rs121908672, LRP5

N. diseases: 3
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.
Worth disease
CUI: C0432273
Disease: Worth disease
3 0.925 0.080 11 68357802 missense variant C/T snv 0.800 1.000 1 2003 2003
Hyperactive behavior
CUI: C0424295
Disease: Hyperactive behavior
112 0.925 0.080 11 68357802 missense variant C/T snv 0.010 1.000 1 2017 2017
Osteogenesis imperfecta type IV (disorder)
CUI: C0268363
Disease: Osteogenesis imperfecta type IV (disorder)
65 0.925 0.080 11 68357802 missense variant C/T snv 0.010 1.000 1 2014 2014