DisGeNET - a database of gene-disease associations

rs57077886, LMNA

N. diseases: 9

Disease: Lipodystrophy ×

Source: ALL

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Gene

Disease

Variant

Source

Association Type

Semantic type

Protein Class

Disease Class

Type

Original DB

Consequence

DSI _v

DPI _v

pLI

EI _vda

EL _gda

Score _vda

PMID

PMID Year

AF_EXOME

Num. PMIDs

Num. SNPs_gda

AF_GENOME

Disease

Risk Allele

Score _vda

Association Type

Original DB

Sentence supporting the association

PMID

PMID Year

Lipodystrophy

CUI:	C0023787
Disease:	Lipodystrophy

0.710

GeneticVariation

BEFREE

Atypical generalized lipoatrophy and severe insulin resistance due to a heterozygous LMNA p.T10I mutation.

2008

Lipodystrophy

CUI:	C0023787
Disease:	Lipodystrophy

0.710

CausalMutation

CLINVAR