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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CDH15
(R60C)
Single nucleotide variant
(missense variant)
Intellectual disability, autosomal dominant 3
+1 more
GLikely benign
CDH15
(R92W)
Single nucleotide variant
(missense variant)
not specified
+1 more
GUncertain significance
CDH15
Single nucleotide variant
(synonymous variant)
Intellectual disability, autosomal dominant 3
+2 more
GBenign/Likely benign
CDH15
(A790V)
Single nucleotide variant
(missense variant)
Intellectual disability, autosomal dominant 3
+2 more
GConflicting classifications of pathogenicity
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