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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
B3GAT3
(V190I +1 more)
Single nucleotide variant
(missense variant +1 more)
B3GAT3-related disorder
+1 more
GUncertain significance
B3GAT3
Single nucleotide variant
(synonymous variant +1 more)
not provided
+2 more
GLikely benign
B3GAT3
Single nucleotide variant
(synonymous variant +1 more)
B3GAT3-related disorder
GLikely benign
B3GAT3
Single nucleotide variant
(synonymous variant +1 more)
Larsen-like syndrome, B3GAT3 type
+1 more
GLikely benign
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