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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TRIO
(I1187V)
Single nucleotide variant
(missense variant +1 more)
Intellectual developmental disorder, autosomal dominant 63, with macrocephaly
+1 more
GUncertain significance
TRIO
(N1465S)
Single nucleotide variant
(missense variant +1 more)
TRIO-Related Disorders
+4 more
GPathogenic/Likely pathogenic
TRIO
(T1668I)
Single nucleotide variant
(missense variant +1 more)
Micrognathia-recurrent infections-behavioral abnormalities-mild intellectual disability syndrome
+1 more
GUncertain significance
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