LAMA1, laminin subunit alpha 1, 284217

N. diseases: 107; N. variants: 21
Disease: Myopia ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1568019012
rs1568019012
Entrez Id: 284217
Gene Symbol: LAMA1
LAMA1
CUI: C0027092
Disease:
Myopia 		A 0.700 CausalMutation CLINVAR