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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PCDH12
(R1124C)
Single nucleotide variant
(missense variant)
Diencephalic-mesencephalic junction dysplasia syndrome 1
+2 more
GUncertain significance
PCDH12
(R1049Q)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
PCDH12, RNF14
(P651A)
Single nucleotide variant
(missense variant)
Diencephalic-mesencephalic junction dysplasia syndrome 1
GUncertain significance
PCDH12, RNF14
(R470W)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+2 more
GUncertain significance
PCDH12, RNF14
(E39*)
Single nucleotide variant
(nonsense)
Diencephalic-mesencephalic junction dysplasia syndrome 1
GLikely pathogenic
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