rs121908673, LRP5

N. diseases: 2
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.
OSTEOPETROSIS, AUTOSOMAL DOMINANT 1
CUI: C1843330
Disease: OSTEOPETROSIS, AUTOSOMAL DOMINANT 1
4 0.925 0.160 11 68363818 missense variant C/T snv 0.800 1.000 1 2003 2003
OVERLAP CONNECTIVE TISSUE DISEASE
CUI: C1858556
Disease: OVERLAP CONNECTIVE TISSUE DISEASE
31 0.925 0.160 11 68363818 missense variant C/T snv 0.010 1.000 1 2005 2005