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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SLC38A8
(R299fs)
Deletion
(frameshift variant)
Foveal hypoplasia - optic nerve decussation defect - anterior segment dysgenesis syndrome
GLikely pathogenic
SLC38A8
(D283A)
Single nucleotide variant
(missense variant)
Foveal hypoplasia - optic nerve decussation defect - anterior segment dysgenesis syndrome
+1 more
GConflicting classifications of pathogenicity
SLC38A8
(Y265C)
Single nucleotide variant
(missense variant)
Foveal hypoplasia - optic nerve decussation defect - anterior segment dysgenesis syndrome
+1 more
GUncertain significance
SLC38A8
(L197F)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
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