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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KDM5B
Single nucleotide variant
(synonymous variant)
Intellectual disability, autosomal recessive 65
+1 more
GBenign
KDM5B
Duplication
(intron variant)
Intellectual disability, autosomal recessive 65
GBenign
KDM5B
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GBenign
KDM5B
Single nucleotide variant
(synonymous variant)
Intellectual disability, autosomal recessive 65
+1 more
GBenign
KDM5B
Single nucleotide variant
(synonymous variant)
Intellectual disability, autosomal recessive 65
+1 more
GBenign
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