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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
HBA2, LOC106804612
(K17E)
Single nucleotide variant
(missense variant)
not provided
GConflicting classifications of pathogenicity
HBA1, LOC106804613
(K17E)
Single nucleotide variant
(missense variant)
not provided
+1 more
GLikely benign