269700.G.1

Lebanon

Lipoatrophy; Hyperlipidemia; Hepatomegaly; Insulin resistance;

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Variant Name	Allele Count	Allele Frequency	Associated Disease	Associated Gene
NM_001122955.3:c.509_513delATCGT	42		Lipodystrophy, Congenital Generalized, Type 2

Group of 21 patients from 6 families