RS267607623 LMNA

Health Risk Chr 1:156136021
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Charcot-Marie-Tooth disease type 2
Cardiovascular phenotype
Neuronopathy
distal hereditary motor
autosomal dominant
Charcot-Marie-Tooth disease type 2
Cardiovascular phenotype
Neuronopathy
distal hereditary motor
autosomal dominant
Other Variants in LMNA
rs61046466 rs58932704 rs28928900 rs57520892 rs60934003 rs28933091 rs28933092 rs80338938 rs11575937 rs57318642
Ask Dr. Hemsworth about this variant