RELN, reelin, 5649

N. diseases: 178; N. variants: 52
Disease: EPILEPSY, FAMILIAL TEMPORAL LOBE, 7 ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs768119894
rs768119894
Entrez Id: 5649
Gene Symbol: RELN
RELN
CUI: C4225327
Disease:
EPILEPSY, FAMILIAL TEMPORAL LOBE, 7 		0.800 GeneticVariation UNIPROT Heterozygous reelin mutations cause autosomal-dominant lateral temporal epilepsy. 26046367 2015
dbSNP: rs768119894
rs768119894
Entrez Id: 5649
Gene Symbol: RELN
RELN
CUI: C4225327
Disease:
EPILEPSY, FAMILIAL TEMPORAL LOBE, 7 		C 0.800 CausalMutation CLINVAR