Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs587778771
rs587778771
PRRT2 ; LOC112268170
GC 0.700 CausalMutation CLINVAR The evolving spectrum of PRRT2-associated paroxysmal diseases. 26598493

2015
dbSNP: rs587778771
rs587778771
PRRT2 ; LOC112268170
GC 0.700 CausalMutation CLINVAR Exome sequencing identifies truncating mutations in PRRT2 that cause paroxysmal kinesigenic dyskinesia. 22101681

2011