C1865974[trait identifier] AND "Genome-Nilou Lab"[submitter] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1283302	NM_017662.5(TRPM6):c.5776+23A>G	TRPM6	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 367301	NM_017662.5(TRPM6):c.4750A>G (p.Lys1584Glu)	TRPM6 (K1584E +1 more)	Single nucleotide variant (missense variant)	Intestinal hypomagnesemia 1 +1 more	GBenign
Select item 367306	NM_017662.5(TRPM6):c.4177G>A (p.Val1393Ile)	TRPM6 (V1393I +1 more)	Single nucleotide variant (missense variant)	Intestinal hypomagnesemia 1 +1 more	GBenign
Select item 367314	NM_017662.5(TRPM6):c.2442G>A (p.Gln814=)	TRPM6	Single nucleotide variant (synonymous variant)	Intestinal hypomagnesemia 1 +1 more	GBenign
Select item 367318	NM_017662.5(TRPM6):c.2124T>G (p.Leu708=)	TRPM6	Single nucleotide variant (synonymous variant)	Intestinal hypomagnesemia 1 +1 more	GBenign
Select item 1237924	NM_017662.5(TRPM6):c.1443+42A>G	TRPM6	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 367327	NM_017662.5(TRPM6):c.954C>T (p.Gly318=)	TRPM6	Single nucleotide variant (synonymous variant)	Intestinal hypomagnesemia 1 +1 more	GBenign

ClinVar