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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PIGN
(F414I)
Single nucleotide variant
(missense variant)
Multiple congenital anomalies-hypotonia-seizures syndrome 1
GUncertain significance
PIGN
(I332M)
Single nucleotide variant
(missense variant)
Multiple congenital anomalies-hypotonia-seizures syndrome 1
+3 more
GConflicting classifications of pathogenicity
PIGN
(L126P)
Single nucleotide variant
(missense variant)
Neurodevelopmental delay
+1 more
GUncertain significance
PIGN
(G104R)
Single nucleotide variant
(missense variant)
Multiple congenital anomalies-hypotonia-seizures syndrome 1
GUncertain significance
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