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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC110006319, LOC107133510
+1 more
(E122Q)
Single nucleotide variant
(missense variant)
Hemoglobin D disease
+5 more
GPathogenic/Likely pathogenic
LOC107133510, LOC110006319
+1 more
Single nucleotide variant
(intron variant)
Beta-thalassemia HBB/LCRB
+10 more
GPathogenic