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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DHX16
(Q216H +2 more)
Single nucleotide variant
(missense variant)
Neuromuscular disease and ocular or auditory anomalies with or without seizures
+4 more
GPathogenic/Likely pathogenic
DDX54
(V286M)
Single nucleotide variant
(missense variant)
DDX54-related disorder
GBenign
DHX34
(Q156*)
Single nucleotide variant
(nonsense)
Neurodevelopmental disorders
+6 more
GLikely pathogenic
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