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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
HBB, LOC106099062
+2 more
Deletion
beta Thalassemia
GPathogenic
HBB, LOC106099062
+1 more
(A14T)
Single nucleotide variant
(missense variant)
beta Thalassemia
GBenign