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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
EIF2B4, GTF3C2-AS2
(R466W +7 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GConflicting classifications of pathogenicity
EIF2B4, GTF3C2-AS2
Single nucleotide variant
(intron variant)
not specified
+2 more
GBenign
EIF2B4, GTF3C2-AS2
Single nucleotide variant
(synonymous variant)
not provided
+2 more
GBenign
EIF2B4, GTF3C2-AS2
Single nucleotide variant
(intron variant)
not specified
+2 more
GBenign
GTF3C2-AS2, EIF2B4
(R306G +7 more)
Single nucleotide variant
(missense variant)
Vanishing white matter disease
+2 more
GBenign
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