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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
NACC1
(K42R)
Single nucleotide variant
(missense variant)
not provided
+1 more
GConflicting classifications of pathogenicity
NACC1
(R298W)
Single nucleotide variant
(missense variant)
not provided
+2 more
GPathogenic/Likely pathogenic
NACC1
(D462N)
Single nucleotide variant
(missense variant)
Neurodevelopmental disorder with epilepsy, cataracts, feeding difficulties, and delayed brain myelination
GLikely pathogenic
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