Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs74315411
rs74315411
PRNP
0.710 GeneticVariation BEFREE Loss of glycosylation associated with the T183A mutation in human prion disease. 15558291

2004
dbSNP: rs74315411
rs74315411
PRNP
G 0.710 CausalMutation CLINVAR