269700.9

Lebanon

Diabetes mellitus; Cardiomyopathy; Decreased serum leptin; Reduced subcutaneous adipose tissue; Intellectual Disability; Cardiomyopathy;

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Male

Variant Name	Allele Count	Allele Frequency	Associated Disease	Associated Gene
NM_001122955.3:c.509_513delATCGT	2		Lipodystrophy, Congenital Generalized, Type 2