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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SETD1B
(D458fs)
Duplication
(frameshift variant)
Intellectual developmental disorder with seizures and language delay
GPathogenic
SETD1B
(S1464P)
Single nucleotide variant
(missense variant)
Intellectual developmental disorder with seizures and language delay
GUncertain significance
SETD1B
Single nucleotide variant
(intron variant)
Intellectual developmental disorder with seizures and language delay
GUncertain significance
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