RS60864230 LMNA
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What This Variant Does
"[OMIM:?]
Associated Conditions
Familial partial lipodystrophy
Dunnigan type
Hutchinson-Gilford progeria syndrome
childhood-onset
Charcot-Marie-Tooth disease type 2
Emery-Dreifuss muscular dystrophy 2
autosomal dominant
Charcot-Marie-Tooth disease type 2
Charcot-Marie-Tooth disease type 2
Lipoatrophy with Diabetes
Hepatic Steatosis
Hypertrophic Cardiomyopathy
and Leukomelanodermic Papules
Charcot-Marie-Tooth disease type 2B1
Familial partial lipodystrophy
Other Variants in LMNA