"Mayo Clinic Laboratories, Mayo Clinic"[submitter] AND "SLC10A2"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2870752	NM_000452.3(SLC10A2):c.1045T>C (p.Ter349Gln)	SLC10A2	Single nucleotide variant (stop lost)	not provided	GUncertain significance
Select item 3380166	NM_000452.3(SLC10A2):c.989C>T (p.Thr330Met)	SLC10A2 (T330M)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2683237	NM_000452.3(SLC10A2):c.790A>G (p.Met264Val)	SLC10A2 (M264V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 242727	NM_000452.3(SLC10A2):c.785C>T (p.Thr262Met)	SLC10A2 (T262M)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 501088	NM_000452.3(SLC10A2):c.425C>T (p.Pro142Leu)	SLC10A2 (P142L)	Single nucleotide variant (missense variant)	not provided	GConflicting classifications of pathogenicity
Select item 595946	NM_000452.3(SLC10A2):c.347C>T (p.Ala116Val)	SLC10A2 (A116V)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 501874	NM_000452.3(SLC10A2):c.132G>C (p.Leu44Phe)	SLC10A2 (L44F)	Single nucleotide variant (missense variant)	Bile acid malabsorption, primary, 1 +1 more	GConflicting classifications of pathogenicity
Select item 1694091	NM_000452.3(SLC10A2):c.118A>G (p.Ile40Val)	SLC10A2 (I40V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance

ClinVar