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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CCDC22
(R384C)
Single nucleotide variant
(missense variant)
not specified
+2 more
GConflicting classifications of pathogenicity
CCDC22
(D546N)
Single nucleotide variant
(missense variant)
not provided
+1 more
GBenign/Likely benign