Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs74315414
rs74315414
PRNP
0.720 GeneticVariation BEFREE Atypical prion protein conformation in familial prion disease with PRNP P105T mutation. 20875062

2011
dbSNP: rs74315414
rs74315414
PRNP
0.720 GeneticVariation BEFREE A novel PRNP-P105S mutation associated with atypical prion disease and a rare PrPSc conformation. 18955686

2008
dbSNP: rs74315414
rs74315414
PRNP
A 0.720 CausalMutation CLINVAR

dbSNP: rs74315414
rs74315414
PRNP
T 0.720 CausalMutation CLINVAR