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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FBXO31
(V450M +1 more)
Single nucleotide variant
(missense variant)
Intellectual disability, autosomal recessive 45
GUncertain significance
FBXO31
Single nucleotide variant
(intron variant)
Intellectual disability, autosomal recessive 45
+1 more
GUncertain significance
FBXO31
(P41H +1 more)
Single nucleotide variant
(missense variant)
Intellectual disability, autosomal recessive 45
GUncertain significance
FBXO31
(G15E)
Single nucleotide variant
(missense variant +1 more)
Intellectual disability, autosomal recessive 45
GUncertain significance
ACSF3, ADAD2
+83 more
Copy number gain
not provided
GPathogenic
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