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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SLC6A19
(A39V)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SLC6A19
(D173N)
Single nucleotide variant
(missense variant)
Neutral 1 amino acid transport defect
+4 more
GConflicting classifications of pathogenicity
SLC6A19
(R214C)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SLC6A19
(R332C)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
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