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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TUBB4B
(R391C)
Single nucleotide variant
(missense variant)
Leber congenital amaurosis with early-onset deafness
+1 more
GConflicting classifications of pathogenicity
TUBB4B
(R391H)
Single nucleotide variant
(missense variant)
Leber congenital amaurosis with early-onset deafness
+1 more
GPathogenic/Likely pathogenic