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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CHD8, LOC126861888
Single nucleotide variant
(synonymous variant)
Inborn genetic diseases
+1 more
GConflicting classifications of pathogenicity
CHD8
Single nucleotide variant
(splice donor variant)
Autism spectrum disorder
+1 more
Gnot provided