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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
UNC5B
(V371M +1 more)
Single nucleotide variant
(missense variant)
UNC5B-related disorder
GLikely benign
UNC5B
(D396N +1 more)
Single nucleotide variant
(missense variant)
UNC5B-related disorder
GLikely benign
UNC5B
(R852H +1 more)
Single nucleotide variant
(missense variant)
UNC5B-related disorder
GLikely benign
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