Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs768562045
rs768562045
PRNP
CUI: C0162534
Disease: Prion Diseases
Prion Diseases 		0.010 GeneticVariation BEFREE Thus, we illustrate the utility of harnessing multiple lines of prion disease-specific evidence in the evaluation of the T201S variant, which may be similarly applied to assess other novel variants in PRNP. 29861043

2018