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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TCN2
(V175M +1 more)
Single nucleotide variant
(missense variant)
TCN2-related condition
+1 more
GConflicting classifications of pathogenicity
TCN2
(S256fs +1 more)
Duplication
(frameshift variant)
Transcobalamin II deficiency
GPathogenic
TCN2
(R413G +1 more)
Single nucleotide variant
(missense variant)
not provided
+2 more
GConflicting classifications of pathogenicity
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