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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
EBF3
(A270fs +1 more)
Duplication
(frameshift variant)
not provided
+1 more
GPathogenic
EBF3
(N197D)
Single nucleotide variant
(missense variant)
Hypotonia, ataxia, and delayed development syndrome
GLikely pathogenic
EBF3
(I183fs)
Deletion
(frameshift variant)
Hypotonia, ataxia, and delayed development syndrome
GLikely pathogenic
EBF3
(D125N)
Single nucleotide variant
(missense variant)
Hypotonia, ataxia, and delayed development syndrome
+1 more
GUncertain significance
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