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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SPTB
(A2023V)
Single nucleotide variant
(missense variant)
Hereditary spherocytosis type 2
+2 more
GConflicting classifications of pathogenicity
SPTB
(K1369E)
Single nucleotide variant
(missense variant)
not provided
+2 more
GConflicting classifications of pathogenicity
SPTB
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GConflicting classifications of pathogenicity
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