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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
STX1B
Single nucleotide variant
(intron variant)
Generalized epilepsy with febrile seizures plus, type 9
GLikely benign
STX1B
Single nucleotide variant
(synonymous variant)
not provided
+2 more
GBenign/Likely benign
STX1B
(A11V)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+1 more
GConflicting classifications of pathogenicity
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