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Items: 11

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CHD2
(Y316*)
Duplication
(nonsense)
not provided
+1 more
GLikely pathogenic
CHD2
(K349fs)
Deletion
(frameshift variant)
Intellectual disability
GPathogenic
CHD2
(T645M)
Single nucleotide variant
(missense variant)
Neurodevelopmental disorder
+2 more
GPathogenic/Likely pathogenic
CHD2
(T647I)
Single nucleotide variant
(missense variant)
Intellectual disability
GLikely pathogenic
CHD2
(R699W)
Single nucleotide variant
(missense variant)
Intellectual disability
+3 more
GConflicting classifications of pathogenicity
CHD2
(E924del)
Microsatellite
(inframe_deletion)
Developmental and epileptic encephalopathy 94
+1 more
GLikely pathogenic
CHD2, LOC126862230
Microsatellite
(frameshift variant)
Developmental and epileptic encephalopathy 94
+1 more
GPathogenic/Likely pathogenic
CHD2
Single nucleotide variant
(splice acceptor variant)
Intellectual disability
GLikely pathogenic
CHD2
(K1391fs)
Deletion
(frameshift variant)
Developmental and epileptic encephalopathy 94
+2 more
GConflicting classifications of pathogenicity
CHD2
(G1450fs)
Deletion
(frameshift variant)
Intellectual disability
GPathogenic
CHD2
(Q1523*)
Single nucleotide variant
(nonsense)
Intellectual disability
+1 more
GPathogenic
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