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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PCDH19
Single nucleotide variant
(synonymous variant)
Inborn genetic diseases
+3 more
GBenign
PCDH19
(V384G)
Single nucleotide variant
(missense variant)
Developmental and epileptic encephalopathy, 1
GUncertain significance
PCDH19
(E308*)
Single nucleotide variant
(nonsense)
Epileptic encephalopathy
GLikely pathogenic
PCDH19
Single nucleotide variant
(synonymous variant)
Developmental and epileptic encephalopathy, 9
+3 more
GBenign
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