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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
HBD, LOC106099063
Single nucleotide variant
(intron variant)
not provided
GUncertain significance
HBD, LOC106099063
(A28S)
Single nucleotide variant
(missense variant)
Fetal hemoglobin quantitative trait locus 1
+2 more
GConflicting classifications of pathogenicity