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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ST3GAL3
Single nucleotide variant
(splice donor variant +1 more)
Early infantile epileptic encephalopathy with suppression bursts
+1 more
GPathogenic/Likely pathogenic
ST3GAL3
Single nucleotide variant
(intron variant)
Early infantile epileptic encephalopathy with suppression bursts
+1 more
GConflicting classifications of pathogenicity
ST3GAL3
(E211K +8 more)
Single nucleotide variant
(missense variant +2 more)
Developmental and epileptic encephalopathy, 15
+1 more
GUncertain significance
KCNT1
(R474H +1 more)
Single nucleotide variant
(missense variant)
not provided
+5 more
GPathogenic/Likely pathogenic
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