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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
STX1B
(I282T)
Single nucleotide variant
(missense variant)
not provided
+2 more
GConflicting classifications of pathogenicity
STX1B
(Y234*)
Insertion
(nonsense)
Generalized epilepsy with febrile seizures plus, type 9
GLikely pathogenic
STX1B
Single nucleotide variant
(splice donor variant)
Generalized epilepsy with febrile seizures plus, type 9
GPathogenic
STX1B
(K116fs)
Duplication
(frameshift variant)
Generalized epilepsy with febrile seizures plus, type 9
GLikely pathogenic
STX1B
Single nucleotide variant
(intron variant)
Generalized epilepsy with febrile seizures plus, type 9
GUncertain significance
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