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Items: 6

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CDH23, CDH23-AS1
Single nucleotide variant
(splice acceptor variant)
not provided
GPathogenic
CDH23, CDH23-AS1
Single nucleotide variant
(synonymous variant)
not specified
+2 more
GBenign/Likely benign
CDH23, CDH23-AS1
(V87L)
Single nucleotide variant
(missense variant)
not specified
+3 more
GUncertain significance
CDH23, CDH23-AS1
(E104K)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
CDH23, CDH23-AS1
Single nucleotide variant
(synonymous variant)
CDH23-related condition
+1 more
GConflicting classifications of pathogenicity
CDH23-AS1, CDH23
(A129T)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+4 more
GUncertain significance
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