RELN, reelin, 5649

N. diseases: 178; N. variants: 52
Disease: Epilepsy, Rolandic ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs200124755
rs200124755
Entrez Id: 5649;101927870
Gene Symbol: RELN;LOC101927870
RELN;LOC101927870
CUI: C0376532
Disease:
Epilepsy, Rolandic 		G 0.700 CausalMutation CLINVAR Exome-wide analysis of mutational burden in patients with typical and atypical Rolandic epilepsy. 29358611 2018