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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
OTUD6B
(L100fs +2 more)
Deletion
(frameshift variant)
Intellectual developmental disorder with dysmorphic facies, seizures, and distal limb anomalies
GPathogenic
OTUD6B
(S179L +1 more)
Single nucleotide variant
(missense variant)
OTUD6B-related condition
+2 more
GConflicting classifications of pathogenicity