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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SLC12A1
Deletion
(splice donor variant)
Bartter disease type 1
GUncertain significance
SLC12A1
(K1032E)
Single nucleotide variant
(missense variant)
Bartter disease type 1
GUncertain significance