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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
HBA2, LOC106804612
(G60R)
Single nucleotide variant
(missense variant)
not provided
+1 more
GLikely pathogenic
HBA2, LOC106804612
(C105Y)
Single nucleotide variant
(missense variant)
Hemoglobin H disease
+2 more
GPathogenic/Likely pathogenic
HBA2, LOC106804612
Single nucleotide variant
(stop lost)
not provided
+2 more
GPathogenic
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