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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
NFIB
(P140A +11 more)
Single nucleotide variant
(missense variant +1 more)
Macrocephaly, acquired, with impaired intellectual development
GUncertain significance
NFIB
(V136M +6 more)
Single nucleotide variant
(missense variant +1 more)
Macrocephaly, acquired, with impaired intellectual development
GUncertain significance
NFIB
(D116fs +6 more)
Deletion
(frameshift variant +1 more)
Inborn genetic diseases
+1 more
GPathogenic/Likely pathogenic
NFIB
(K3fs +6 more)
Deletion
(frameshift variant)
Macrocephaly, acquired, with impaired intellectual development
GLikely pathogenic
NFIB
Single nucleotide variant
(intron variant)
Macrocephaly, acquired, with impaired intellectual development
GUncertain significance
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