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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SLC12A3
(G850S +2 more)
Single nucleotide variant
(missense variant)
Familial hypokalemia-hypomagnesemia
GUncertain significance
SLC12A3
(R861C +2 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GPathogenic