Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs28933385
rs28933385
PRNP
0.020 GeneticVariation BEFREE Characterization of sleep disorders in patients with E200K familial Creutzfeldt-Jakob disease. 25451855

2015
dbSNP: rs28933385
rs28933385
PRNP
0.020 GeneticVariation BEFREE A missense mutation in codon 200 (E200K) of the PRNP was identified in this patient; CSF 14-3-3 protein was positive; sleep disturbance was the initial sign and the other symptoms gradually appeared, including memory loss, dizziness and ataxia. 20514992

2010