RS267607600 LMNA

Health Risk Chr 1:156136919
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What This Variant Does
"CLNSIG=4
Associated Conditions
Congenital muscular dystrophy due to LMNA mutation
Cardiovascular phenotype
Emery-Dreifuss muscular dystrophy 2
autosomal dominant
Congenital muscular dystrophy due to LMNA mutation
Cardiovascular phenotype
Emery-Dreifuss muscular dystrophy 2
autosomal dominant
Other Variants in LMNA
rs61046466 rs58932704 rs28928900 rs57520892 rs60934003 rs28933091 rs28933092 rs80338938 rs11575937 rs57318642
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