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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SLC6A19
(D173N)
Single nucleotide variant
(missense variant)
SLC6A19-related condition
+5 more
GConflicting classifications of pathogenicity
SLC6A19
(M432fs)
Deletion
(frameshift variant)
not provided
GConflicting classifications of pathogenicity