Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs74315407
rs74315407
PRNP
0.720 GeneticVariation BEFREE Interestingly, type of prion disease (sporadic vs. genetic) and the PRNP mutation (E200K vs. V210I and FFI), codon 129 genotype, and PrP(Sc) type affected RT-QuIC response. 24809690

2015
dbSNP: rs74315407
rs74315407
PRNP
0.720 GeneticVariation BEFREE Toward the molecular basis of inherited prion diseases: NMR structure of the human prion protein with V210I mutation. 21839748

2011
dbSNP: rs74315407
rs74315407
PRNP
A 0.720 CausalMutation CLINVAR