Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs57077886
rs57077886
LMNA
CUI: C0023787
Disease: Lipodystrophy
Lipodystrophy 		0.710 GeneticVariation BEFREE Atypical generalized lipoatrophy and severe insulin resistance due to a heterozygous LMNA p.T10I mutation. 19169477

2008
dbSNP: rs57077886
rs57077886
LMNA
CUI: C0023787
Disease: Lipodystrophy
Lipodystrophy 		T 0.710 CausalMutation CLINVAR