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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
NBEA
Single nucleotide variant
(synonymous variant)
Neurodevelopmental disorder with or without early-onset generalized epilepsy
+1 more
GBenign/Likely benign
NBEA
(R1278Q)
Single nucleotide variant
(missense variant)
not provided
GLikely benign
NBEA
Single nucleotide variant
(synonymous variant)
not provided
GBenign/Likely benign
NBEA
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
NBEA
(V2784F +3 more)
Single nucleotide variant
(missense variant)
not provided
GBenign
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