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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SLC12A3
Single nucleotide variant
(splice donor variant)
not provided
+1 more
GPathogenic
SLC12A3
(R642G +1 more)
Single nucleotide variant
(missense variant)
Familial hypokalemia-hypomagnesemia
+1 more
GPathogenic/Likely pathogenic
SLC12A3
(P643L +1 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GPathogenic/Likely pathogenic
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