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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SPTB
(T2040I)
Single nucleotide variant
(missense variant)
Hereditary spherocytosis type 2
GLikely pathogenic
SPTB
(F2014C)
Single nucleotide variant
(missense variant)
Elliptocytosis 3
GUncertain significance