rs1403967930
This variant is located in the AHSG gene.
▶ClinVar annotation
About AHSG
The protein encoded by this gene is a negatively-charged serum glycoprotein that is synthesized by hepatocytes. The encoded protein consists of two polypeptide chains, which are both cleaved from a proprotein encoded from a single mRNA. It is involved in several processes, including endocytosis, brain development, and the formation of bone tissue. Defects in this gene are a cause of susceptibility to leanness. [provided by RefSeq, Aug 2017]
View all AHSG variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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