RELN, reelin, 5649

N. diseases: 178; N. variants: 52
Disease: LISSENCEPHALY SYNDROME, NORMAN-ROBERTS TYPE ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs587780436
rs587780436
Entrez Id: 5649
Gene Symbol: RELN
RELN
CUI: C0796089
Disease:
LISSENCEPHALY SYNDROME, NORMAN-ROBERTS TYPE 		TGGTGGAGAGTGGAA 0.700 CausalMutation CLINVAR