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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CLCNKA, LOC106501712
(E586* +2 more)
Single nucleotide variant
(nonsense)
Bartter disease type 4B
GLikely pathogenic
CLCNKA, LOC106501712
(V657M +2 more)
Single nucleotide variant
(missense variant)
Bartter disease type 4B
+1 more
GUncertain significance