Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs767181086
rs767181086
LAMC2
CUI: C0162534
Disease: Prion Diseases
Prion Diseases 		0.010 GeneticVariation BEFREE Genetic Creutzfeldt-Jakob disease (gCJD) with E200K mutation is one of the common subtypes of human genetic prion diseases worldwide. 30755683

2019