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Items: 15

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FOXE3, LINC01389
Single nucleotide variant
(5 prime UTR variant)
not specified
+1 more
GBenign
FOXE3, LINC01389
(D6N)
Single nucleotide variant
(missense variant)
Anterior segment dysgenesis
+4 more
GBenign/Likely benign
FOXE3, LINC01389
(E36K)
Single nucleotide variant
(missense variant)
Anterior segment dysgenesis
+3 more
GUncertain significance
FOXE3, LINC01389
(E43A)
Single nucleotide variant
(missense variant)
Congenital primary aphakia
+2 more
GUncertain significance
FOXE3, LINC01389
Single nucleotide variant
(synonymous variant)
not provided
GUncertain significance
FOXE3, LINC01389
(G47C)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
FOXE3, LINC01389
(G49A)
Single nucleotide variant
(missense variant)
Anterior segment dysgenesis
+5 more
GBenign
LINC01389, FOXE3
Single nucleotide variant
(synonymous variant)
not provided
GUncertain significance
FOXE3, LINC01389
(R99C)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
FOXE3, LINC01389
Single nucleotide variant
(synonymous variant)
Anterior segment dysgenesis
+4 more
GBenign
LINC01389, FOXE3
Single nucleotide variant
(synonymous variant)
Cardiovascular phenotype
+7 more
GBenign
FOXE3, LINC01389
Single nucleotide variant
(synonymous variant)
Cardiovascular phenotype
+4 more
GBenign
FOXE3, LINC01389
Single nucleotide variant
(synonymous variant)
Cardiovascular phenotype
+3 more
GConflicting classifications of pathogenicity
FOXE3, LINC01389
(S300G)
Single nucleotide variant
(missense variant)
Anterior segment dysgenesis
+5 more
GBenign/Likely benign
FOXE3, LINC01389
(G310D)
Single nucleotide variant
(missense variant)
Anterior segment dysgenesis
+4 more
GBenign/Likely benign
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