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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LMNA, LOC129931597
(A14E)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
LMNA, LOC129931597
Single nucleotide variant
(synonymous variant)
Cardiomyopathy
+20 more
GBenign/Likely benign
LMNA, LOC129931597
(S22L)
Single nucleotide variant
(missense variant)
not provided
+14 more
GConflicting classifications of pathogenicity
LMNA, LOC129931597
(E33D)
Single nucleotide variant
(missense variant)
not provided
+1 more
GConflicting classifications of pathogenicity
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