"Baylor Genetics"[submitter] AND "CLDN16"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1028522	NM_006580.4(CLDN16):c.2T>C (p.Met1Thr)	CLDN16 (M1T)	Single nucleotide variant (missense variant +1 more)	Primary hypomagnesemia	GConflicting classifications of pathogenicity
Select item 1028524	NM_006580.4(CLDN16):c.218-10G>A	CLDN16	Single nucleotide variant (intron variant)	Primary hypomagnesemia	GUncertain significance
Select item 5925	NM_006580.4(CLDN16):c.235C>T (p.Arg79Ter)	CLDN16 (R149* +1 more)	Single nucleotide variant (nonsense)	not provided +1 more	GPathogenic

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