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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SPTA1
(H1755D)
Single nucleotide variant
(missense variant)
Hereditary spherocytosis type 3
GLikely pathogenic
SPTA1
(T540N)
Single nucleotide variant
(missense variant)
Elliptocytosis 2
GUncertain significance