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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CSNK2A1
(K198R +1 more)
Single nucleotide variant
(missense variant)
See cases
+4 more
GPathogenic/Likely pathogenic
CSNK2A1
(R47Q)
Single nucleotide variant
(missense variant +1 more)
Okur-Chung neurodevelopmental syndrome
+1 more
GPathogenic/Likely pathogenic