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Links from MedGen

Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CNOT2
(P116S +4 more)
Single nucleotide variant
(missense variant +1 more)
Intellectual developmental disorder with nasal speech, dysmorphic facies, and variable skeletal anomalies
GUncertain significance
CNOT2
(K316*)
Single nucleotide variant
(nonsense +1 more)
Intellectual developmental disorder with nasal speech, dysmorphic facies, and variable skeletal anomalies
GPathogenic
CNOT2
Deletion
Intellectual developmental disorder with nasal speech, dysmorphic facies, and variable skeletal anomalies
GPathogenic
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