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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CSNK2A1
(R142* +1 more)
Single nucleotide variant
(nonsense)
Okur-Chung neurodevelopmental syndrome
GPathogenic
CSNK2A1
(S51R)
Single nucleotide variant
(missense variant +1 more)
Okur-Chung neurodevelopmental syndrome
GLikely pathogenic
CSNK2A1
(R47Q)
Single nucleotide variant
(missense variant +1 more)
Okur-Chung neurodevelopmental syndrome
+1 more
GPathogenic/Likely pathogenic
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