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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DEAF1
(D269G +1 more)
Single nucleotide variant
(synonymous variant +1 more)
Intellectual disability
GLikely benign
DEAF1
(G220S)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
+2 more
GConflicting classifications of pathogenicity