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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
HBB, LOC106099062
+1 more
(C94fs)
Insertion
(frameshift variant)
not provided
GPathogenic
HBB, LOC106099062
+1 more
Single nucleotide variant
(intron variant)
not provided
GLikely benign
HBB, LOC106099062
+1 more
Single nucleotide variant
Thalassemia
GUncertain significance
HBB, LOC106099062
+1 more
Single nucleotide variant
Beta-thalassemia HBB/LCRB
GUncertain significance
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