LMNA, lamin A/C, 4000

N. diseases: 824; N. variants: 285
Disease: Atrial Fibrillation ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs58912633
rs58912633
Entrez Id: 4000
Gene Symbol: LMNA
LMNA
CUI: C0004238
Disease:
Atrial Fibrillation 		0.010 GeneticVariation BEFREE Progeria caused by a rare LMNA mutation p.S143F associated with mild myopathy and atrial fibrillation. 18339564 2008