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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CHD8
(P1598S +1 more)
Single nucleotide variant
(missense variant)
Intellectual developmental disorder with autism and macrocephaly
GUncertain significance
CHD8
(R664C +1 more)
Single nucleotide variant
(missense variant)
Intellectual developmental disorder with autism and macrocephaly
GUncertain significance
CHD8
Deletion
(nonsense)
Intellectual developmental disorder with autism and macrocephaly
GLikely pathogenic
CHD8
(Q331* +1 more)
Single nucleotide variant
(nonsense)
Intellectual developmental disorder with autism and macrocephaly
GPathogenic
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