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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CEP104, LOC126805586
(R656C)
Single nucleotide variant
(missense variant)
not provided
+1 more
GBenign/Likely benign
CEP104, LOC126805586
Single nucleotide variant
(synonymous variant)
CEP104-related disorder
+2 more
GBenign/Likely benign