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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SLC52A3
(L442fs)
Deletion
(frameshift variant)
not provided
GLikely pathogenic
SLC52A3
(F113L)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SLC52A3
(R65Q)
Single nucleotide variant
(missense variant)
Brown-Vialetto-van Laere syndrome 1
+2 more
GConflicting classifications of pathogenicity
SLC52A3
(W24*)
Single nucleotide variant
(nonsense)
not provided
GPathogenic
SLC52A3
(N21S)
Single nucleotide variant
(missense variant)
not provided
+4 more
GConflicting classifications of pathogenicity
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