rs57077886, LMNA

N. diseases: 9
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Lipoatrophy
CUI: C1280433
Disease: Lipoatrophy
0.010 GeneticVariation BEFREE Atypical generalized lipoatrophy and severe insulin resistance due to a heterozygous LMNA p.T10I mutation. 19169477 2008