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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SLC12A3
(N406H +1 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GConflicting classifications of pathogenicity
SLC12A3
(A569V +1 more)
Single nucleotide variant
(missense variant)
Familial hypokalemia-hypomagnesemia
+1 more
GUncertain significance
SLC12A3
(V578M +1 more)
Single nucleotide variant
(missense variant)
Familial hypokalemia-hypomagnesemia
+2 more
GConflicting classifications of pathogenicity
SLC12A3
(L858H +2 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GPathogenic
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