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Items: 6

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LGI1
(A12S)
Single nucleotide variant
(missense variant +1 more)
Autosomal dominant epilepsy with auditory features
+1 more
GUncertain significance
LGI1
Single nucleotide variant
(intron variant)
not provided
+2 more
GBenign/Likely benign
LGI1
Single nucleotide variant
(synonymous variant +1 more)
not provided
+1 more
GConflicting classifications of pathogenicity
LGI1
Single nucleotide variant
(synonymous variant +1 more)
Autosomal dominant epilepsy with auditory features
+3 more
GConflicting classifications of pathogenicity
LGI1
Single nucleotide variant
(synonymous variant +1 more)
Autosomal dominant epilepsy with auditory features
+4 more
GConflicting classifications of pathogenicity
LGI1
Single nucleotide variant
(synonymous variant +2 more)
Autosomal dominant epilepsy with auditory features
+2 more
GConflicting classifications of pathogenicity
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