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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SLC19A3
(T422A)
Single nucleotide variant
(missense variant)
Thiamine metabolism dysfunction syndrome 2 (biotin/thiamine-responsive basal ganglia disease type)
+3 more
GPathogenic
SLC19A3
(Q418E)
Single nucleotide variant
(missense variant)
Biotin-responsive basal ganglia disease
+2 more
GConflicting classifications of pathogenicity
SLC19A3
Single nucleotide variant
(intron variant)
not provided
+1 more
GPathogenic/Likely pathogenic
SLC19A3
(G223S +1 more)
Single nucleotide variant
(missense variant)
Biotin-responsive basal ganglia disease
GUncertain significance
SLC19A3
(W55R +1 more)
Single nucleotide variant
(missense variant)
Biotin-responsive basal ganglia disease
GUncertain significance
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