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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SLC2A1
(L162V)
Single nucleotide variant
(missense variant)
Hereditary cryohydrocytosis with reduced stomatin
GUncertain significance
SLC2A1
(G84S)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+6 more
GUncertain significance