← Glossary
Marker

rs6259

rs6259 is a missense variant in exon 8 of the SHBG gene (Asp327Asn, also numbered Asp356Asn depending on whether the signal peptide is counted) that introduces a new N-linked glycosylation site in the laminin G-like domain of sex hormone-binding globulin. The extra glycosylation does not change SHBG's steroid-binding affinity but slows its clearance from the bloodstream, so the Asn allele is associated with higher circulating SHBG levels. Because SHBG binds and limits the free, bioavailable fraction of testosterone and estradiol, this variant underlies the Sex-hormone transport trait.

Traits rs6259 reads

Gene

Reference databases

How Biome reads this

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This page is for educational purposes only and is not medical advice. It is not intended to diagnose, treat, cure, or prevent any disease. Genetic results describe tendencies and predispositions, not diagnoses. Always consult a licensed clinician before making decisions about your health, medications, or supplements.