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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KMT5B
(R540Q +2 more)
Single nucleotide variant
(missense variant)
Intellectual disability, autosomal dominant 51
GUncertain significance
KMT5B
(A513V +2 more)
Single nucleotide variant
(missense variant)
Intellectual disability, autosomal dominant 51
GUncertain significance
KMT5B
(W264S +4 more)
Single nucleotide variant
(missense variant +1 more)
Intellectual disability, autosomal dominant 51
GUncertain significance
KMT5B
(R187* +3 more)
Single nucleotide variant
(nonsense +2 more)
Neural tube defect
+1 more
GPathogenic/Likely pathogenic
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