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Items: 6

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ALDH3A2
(G109E)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
ALDH3A2
(R177*)
Single nucleotide variant
(nonsense +1 more)
not provided
+1 more
GPathogenic/Likely pathogenic
ALDH3A2
(P315S +1 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GPathogenic/Likely pathogenic
ALDH3A2
Single nucleotide variant
(intron variant)
ALDH3A2-related condition
+1 more
GConflicting classifications of pathogenicity
ALDH3A2
(R423C +1 more)
Single nucleotide variant
(missense variant +1 more)
not provided
GConflicting classifications of pathogenicity
ALDH3A2
(P424S +1 more)
Single nucleotide variant
(missense variant +1 more)
not provided
+3 more
GBenign/Likely benign
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