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Items: 7

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
HBZ, LOC106804612
+4 more
Deletion
alpha Thalassemia
GPathogenic
HBA1, HBA2
+2 more
Deletion
alpha Thalassemia
GPathogenic
HBA1, HBA2
+2 more
Deletion
alpha Thalassemia
GPathogenic
HBA1, HBA2
+2 more
Deletion
alpha Thalassemia
GPathogenic
HBA1, HBA2
+1 more
Single nucleotide variant
(stop lost)
not provided
+4 more
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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