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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LMNA, LOC126805877
Single nucleotide variant
(synonymous variant)
Primary dilated cardiomyopathy
+17 more
GConflicting classifications of pathogenicity
LOC126805877, LMNA
(R133Q +2 more)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+14 more
GConflicting classifications of pathogenicity
LMNA, LOC126805877
Single nucleotide variant
(synonymous variant)
Cardiomyopathy
+14 more
GConflicting classifications of pathogenicity
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