LMNB2, lamin B2, 84823

N. diseases: 74; N. variants: 3
Disease: LIPODYSTROPHY, PARTIAL, ACQUIRED, SUSCEPTIBILITY TO ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs57521499
rs57521499
Entrez Id: 84823
Gene Symbol: LMNB2
LMNB2
CUI: C3887501
Disease:
LIPODYSTROPHY, PARTIAL, ACQUIRED, SUSCEPTIBILITY TO 		0.700 GeneticVariation UNIPROT A Chinese patient with acquired partial lipodystrophy caused by a novel mutation with LMNB2 gene. 22768673 2012
dbSNP: rs57521499
rs57521499
Entrez Id: 84823
Gene Symbol: LMNB2
LMNB2
CUI: C3887501
Disease:
LIPODYSTROPHY, PARTIAL, ACQUIRED, SUSCEPTIBILITY TO 		0.700 GeneticVariation UNIPROT Sequencing of the reannotated LMNB2 gene reveals novel mutations in patients with acquired partial lipodystrophy. 16826530 2006