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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
NEXN
(E213del +1 more)
Microsatellite
(inframe_deletion +1 more)
not provided
GUncertain significance
NEXN
(K214N +1 more)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy 2
Gnot provided
NEXN
(R411T +1 more)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy 2
Gnot provided
NEXN
(A412P +1 more)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy 2
Gnot provided
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