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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FCN1
Single nucleotide variant
(synonymous variant)
FCN1-related disorder
GLikely benign
FCN1
Single nucleotide variant
(synonymous variant)
FCN1-related disorder
GLikely benign
FCN1
(G76S)
Single nucleotide variant
(missense variant)
FCN1-related disorder
GUncertain significance
FCN1
(D45E)
Single nucleotide variant
(missense variant)
FCN1-related disorder
GUncertain significance
FCN1
Single nucleotide variant
(synonymous variant)
FCN1-related disorder
GLikely benign
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