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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PIGN
(R709Q)
Single nucleotide variant
(missense variant)
Multiple congenital anomalies-hypotonia-seizures syndrome 1
GPathogenic
PIGN
(H218Q)
Single nucleotide variant
(missense variant)
not provided
+1 more
GLikely pathogenic