rs761296441
This variant is located in the SLC9A9 gene.
▶ClinVar annotation
About SLC9A9
This gene encodes a sodium/proton exchanger that is a member of the solute carrier 9 protein family. The encoded protein localizes the to the late recycling endosomes and may play an important role in maintaining cation homeostasis. Mutations in this gene are associated with autism susceptibility 16 and attention-deficit/hyperactivity disorder. [provided by RefSeq, Mar 2012]
View all SLC9A9 variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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