rs7213707
This variant is located in the SPNS2 gene.
▶ClinVar annotation
About SPNS2
The protein encoded by this gene is a transporter of sphingosine 1-phosphate, a secreted lipid that is important in cardiovascular, immunological, and neural development. Defects in this gene are a cause of early onset progressive hearing loss. [provided by RefSeq, Jul 2016]
View all SPNS2 variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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