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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ACSL4
(N343T +1 more)
Single nucleotide variant
(missense variant)
Intellectual disability, X-linked 63
GUncertain significance
ACSL4
(G269* +1 more)
Single nucleotide variant
(nonsense)
Intellectual disability, X-linked 63
GUncertain significance
ACSL4
(I30M +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+2 more
GConflicting classifications of pathogenicity
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