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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DLD
(G229C +3 more)
Single nucleotide variant
(missense variant)
DLD-Related Disorders
+3 more
GPathogenic
ARMC10, ASB4
+504 more
Inversion
Childhood apraxia of speech
GPathogenic