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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
NR2F1, NR2F1-AS1
(S108N)
Single nucleotide variant
(missense variant)
Neurodevelopmental delay
GLikely pathogenic
NR2F1
(R235L)
Single nucleotide variant
(missense variant)
Neurodevelopmental delay
GPathogenic