LMNA, lamin A/C, 4000

N. diseases: 824; N. variants: 285
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs56793579
rs56793579
Entrez Id: 4000
Gene Symbol: LMNA
LMNA
CUI: C0004238
Disease:
Atrial Fibrillation
0.010 GeneticVariation BEFREE Affected subjects belonging to the pedigree with heterozygous R62G mutation had atrial fibrillation and required pacemaker implantation. 20041886 2010