rs776740117
This variant is located in the SLC22A9 gene.
▶ClinVar annotation
About SLC22A9
Enables short-chain fatty acid transmembrane transporter activity and sodium-independent organic anion transmembrane transporter activity. Involved in hormone transport; short-chain fatty acid transmembrane transport; and sodium-independent organic anion transport. Located in basolateral plasma membrane. Implicated in Lynch syndrome and mismatch repair cancer syndrome. [provided by Alliance of Genome Resources, Jul 2025]
View all SLC22A9 variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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