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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
NEXN
(E212K +1 more)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy
GLikely benign
NEXN
(R328Q +1 more)
Single nucleotide variant
(missense variant)
Primary dilated cardiomyopathy
GUncertain significance
NEXN
(Q349R +1 more)
Single nucleotide variant
(missense variant)
Primary dilated cardiomyopathy
GUncertain significance
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