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Items: 6

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
HBM, HBZ
+4 more
Deletion
alpha Thalassemia
GPathogenic
HBA1, HBA2
+2 more
Deletion
alpha Thalassemia
GPathogenic
LOC106804613, HBA1
+2 more
Deletion
alpha Thalassemia
GPathogenic
LOC106804613, HBA1
+2 more
Deletion
alpha Thalassemia
GPathogenic
HBA1, LOC106804613
(N69K)
Single nucleotide variant
(missense variant)
alpha Thalassemia
Gnot provided
HBA1, LOC106804613
(D75H)
Single nucleotide variant
(missense variant)
not provided
GConflicting classifications of pathogenicity
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