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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ACD
(R27Q)
Single nucleotide variant
(missense variant)
not provided
+2 more
GBenign/Likely benign
ACD
(V8I)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+4 more
GConflicting classifications of pathogenicity