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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
NFIB
(L132P +6 more)
Single nucleotide variant
(missense variant +1 more)
Macrocephaly, acquired, with impaired intellectual development
+2 more
GPathogenic/Likely pathogenic
NFIB
(K126E +6 more)
Single nucleotide variant
(missense variant +1 more)
Macrocephaly, acquired, with impaired intellectual development
+3 more
GPathogenic/Likely pathogenic
NFIB
(R89* +6 more)
Single nucleotide variant
(nonsense)
Macrocephaly, acquired, with impaired intellectual development
+3 more
GConflicting classifications of pathogenicity
NFIB
(R37* +5 more)
Single nucleotide variant
(nonsense +1 more)
Macrocephaly, acquired, with impaired intellectual development
+3 more
GPathogenic
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