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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SLC14A1
(K170fs +3 more)
Deletion
(frameshift variant)
BLOOD GROUP--KIDD SYSTEM
GUncertain significance
SLC14A1
(A138E +3 more)
Single nucleotide variant
(missense variant)
altered red cell phenotype
GAffects