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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ASAH1
(T270M +3 more)
Single nucleotide variant
(missense variant)
Farber lipogranulomatosis
+2 more
GConflicting classifications of pathogenicity
ASAH1
(R349G +3 more)
Single nucleotide variant
(missense variant)
Abnormality of metabolism/homeostasis
+2 more
GConflicting classifications of pathogenicity
ASAH1
(M210T +3 more)
Single nucleotide variant
(missense variant)
not provided
+4 more
GConflicting classifications of pathogenicity
ASAH1
(Y223F +3 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+2 more
GUncertain significance
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