RS57318642 LMNA

Health Risk Chr 1:156137203
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What This Variant Does
"[OMIM:?]
Associated Conditions
Mandibuloacral dysplasia with type A lipodystrophy
Hutchinson-Gilford syndrome
Cardiomyopathy
Charcot-Marie-Tooth disease type 2
Congenital muscular dystrophy due to LMNA mutation
Primary dilated cardiomyopathy
Dilated cardiomyopathy 1A
Mandibuloacral dysplasia with type A lipodystrophy
Hutchinson-Gilford syndrome
Cardiomyopathy
Charcot-Marie-Tooth disease type 2
Congenital muscular dystrophy due to LMNA mutation
Primary dilated cardiomyopathy
Dilated cardiomyopathy 1A
Other Variants in LMNA
rs61046466 rs58932704 rs28928900 rs57520892 rs60934003 rs28933091 rs28933092 rs80338938 rs11575937 rs60864230
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