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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ALAD
Single nucleotide variant
(3 prime UTR variant)
not provided
+1 more
GConflicting classifications of pathogenicity
ALAD
Single nucleotide variant
(synonymous variant)
Porphobilinogen synthase deficiency
+1 more
GBenign/Likely benign
ALAD
Single nucleotide variant
(synonymous variant)
not provided
GBenign/Likely benign
ALAD
(V6I +1 more)
Single nucleotide variant
(missense variant +1 more)
not provided
+1 more
GConflicting classifications of pathogenicity
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