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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LMNA
(K78N)
Single nucleotide variant
(missense variant)
Arrhythmogenic right ventricular dysplasia 9
GLikely pathogenic
LMNA
(L102P)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+2 more
GConflicting classifications of pathogenicity
LMNA
(R249Q +2 more)
Single nucleotide variant
(missense variant)
Abnormality of the musculature
+7 more
GPathogenic/Likely pathogenic
LMNA
(D357V +2 more)
Single nucleotide variant
(missense variant)
Dilated cardiomyopathy 1A
GUncertain significance
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