Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1555790846
rs1555790846
Entrez Id: 23236
Gene Symbol: PLCB1
PLCB1
CUI: C0376532
Disease:
Epilepsy, Rolandic
T 0.700 CausalMutation CLINVAR Exome-wide analysis of mutational burden in patients with typical and atypical Rolandic epilepsy. 29358611 2018