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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
HBA2, LOC106804612
Single nucleotide variant
Thalassemia
GUncertain significance
HBA2, LOC106804612
Single nucleotide variant
(3 prime UTR variant)
Thalassemia
GUncertain significance
HBA2
Single nucleotide variant
not provided
GUncertain significance
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