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Links from Gene

Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CDH2
Single nucleotide variant
(intron variant)
Agenesis of corpus callosum, cardiac, ocular, and genital syndrome
GUncertain significance
CDH2
(R777* +1 more)
Single nucleotide variant
(nonsense)
not provided
GUncertain significance
CDH2
(N212S +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
CDH2
(S613P +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
CDH2
Copy number gain
See cases
GLikely benign
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