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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PIGN
(Y895*)
Single nucleotide variant
(nonsense)
not provided
GUncertain significance
PIGN
Single nucleotide variant
(splice acceptor variant)
not provided
GUncertain significance
PIGN
Single nucleotide variant
(splice donor variant)
not provided
GUncertain significance
PIGN
(R45del)
Microsatellite
(inframe_deletion)
Multiple congenital anomalies-hypotonia-seizures syndrome 1
GUncertain significance
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