"Diagnostic Laboratory, Department of Genetics, University Medical Cen - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 504886	NM_001126108.2(SLC12A3):c.791C>G (p.Ala264Gly)	SLC12A3 (A264G +1 more)	Single nucleotide variant (missense variant)	Familial hypokalemia-hypomagnesemia +2 more	GBenign
Select item 255880	NM_001126108.2(SLC12A3):c.1670-8T>C	SLC12A3	Single nucleotide variant (intron variant)	Familial hypokalemia-hypomagnesemia +2 more	GBenign
Select item 255891	NM_001126108.2(SLC12A3):c.2924+13C>T	SLC12A3	Single nucleotide variant (intron variant)	not specified +2 more	GBenign

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