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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KDM4B
Microsatellite
(inframe_indel +1 more)
Intellectual developmental disorder, autosomal dominant 65
GUncertain significance
KDM4B, LOC130063244
(G592R +1 more)
Single nucleotide variant
(missense variant)
Intellectual developmental disorder, autosomal dominant 65
GUncertain significance
KDM4B
(A651D +1 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
KDM4B
(G782D +1 more)
Single nucleotide variant
(missense variant)
Intellectual developmental disorder, autosomal dominant 65
GUncertain significance
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