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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CHD8
(G1917S +1 more)
Single nucleotide variant
(missense variant)
Intellectual developmental disorder with autism and macrocephaly
GUncertain significance
CHD8
(R1337* +1 more)
Single nucleotide variant
(nonsense)
not provided
+1 more
GPathogenic
CHD8
(P348R +1 more)
Single nucleotide variant
(missense variant)
Intellectual developmental disorder with autism and macrocephaly
GUncertain significance
CHD8
(V344M +1 more)
Single nucleotide variant
(missense variant)
Intellectual developmental disorder with autism and macrocephaly
+1 more
GUncertain significance
CHD8
(G137D)
Single nucleotide variant
(missense variant +1 more)
not provided
+1 more
GUncertain significance
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