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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ANK1, LOC126860368
(R1502H +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ANK1, LOC126860368
Deletion
(nonsense)
not provided
GLikely pathogenic
ANK1, LOC126860368
(R1491H +1 more)
Single nucleotide variant
(missense variant)
Hereditary spherocytosis type 1
+2 more
GUncertain significance
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