Source: UNIPROT

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121908670
rs121908670
LRP5
CUI: C0432273
Disease: Worth disease
Worth disease 		0.800 GeneticVariation UNIPROT Six novel missense mutations in the LDL receptor-related protein 5 (LRP5) gene in different conditions with an increased bone density. 12579474

2003
dbSNP: rs121908671
rs121908671
LRP5
CUI: C0432273
Disease: Worth disease
Worth disease 		0.800 GeneticVariation UNIPROT Six novel missense mutations in the LDL receptor-related protein 5 (LRP5) gene in different conditions with an increased bone density. 12579474

2003
dbSNP: rs121908672
rs121908672
LRP5
CUI: C0432273
Disease: Worth disease
Worth disease 		0.800 GeneticVariation UNIPROT Six novel missense mutations in the LDL receptor-related protein 5 (LRP5) gene in different conditions with an increased bone density. 12579474

2003