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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
STX1B
Single nucleotide variant
(3 prime UTR variant)
Generalized epilepsy with febrile seizures plus, type 9
GUncertain significance
STX1B
Single nucleotide variant
(3 prime UTR variant)
Generalized epilepsy with febrile seizures plus, type 9
GUncertain significance
STX1B
(V88F)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
STX1B
(I43F)
Single nucleotide variant
(missense variant)
Generalized epilepsy with febrile seizures plus, type 9
GUncertain significance
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