rs2039621213
This variant is located in the S1PR2 gene.
▶ClinVar annotation
About S1PR2
This gene encodes a member of the G protein-coupled receptors, as well as the EDG family of proteins. The encoded protein is a receptor for sphingosine 1-phosphate, which participates in cell proliferation, survival, and transcriptional activation. Defects in this gene have been associated with congenital profound deafness. [provided by RefSeq, Mar 2016]
View all S1PR2 variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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