LAMA2, laminin subunit alpha 2, 3908

N. diseases: 167; N. variants: 127
Disease: Seizures ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs145465528
rs145465528
Entrez Id: 3908
Gene Symbol: LAMA2
LAMA2
CUI: C0036572
Disease:
Seizures 		T 0.700 GeneticVariation CLINVAR