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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ASAH1
(R349G +3 more)
Single nucleotide variant
(missense variant)
not provided
+2 more
GPathogenic/Likely pathogenic
ASAH1
(W185R +3 more)
Single nucleotide variant
(missense variant)
Farber lipogranulomatosis
+1 more
GPathogenic/Likely pathogenic
ASAH1
(T42M +2 more)
Single nucleotide variant
(missense variant +1 more)
ASAH1-related disorder
+2 more
GPathogenic/Likely pathogenic
ASAH1
(T42A +1 more)
Single nucleotide variant
(missense variant +1 more)
not provided
+1 more
GConflicting classifications of pathogenicity
ASAH1
(P26L)
Single nucleotide variant
(missense variant +1 more)
Farber lipogranulomatosis
GUncertain significance
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