Standard

Androgen levels

SHBG · rs72829446

What each result means

C/C Published research associates this genotype with typical/baseline likelihood of Androgen levels — no copies of the reported risk allele. (GWAS Catalog, Hum Mol Genet 2012, PMID:22936694)
C/T Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Androgen levels. (GWAS Catalog, Hum Mol Genet 2012, PMID:22936694)
T/T Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Androgen levels compared to the general population. (GWAS Catalog, Hum Mol Genet 2012, PMID:22936694)
Source

Questions about rs72829446

What is rs72829446?

rs72829446 is a single position in the genome, in or near the SHBG gene. Published research associates it with androgen levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs72829446 mean I will get this?

No. Common variants like this one move a probability slightly and, on their own, rarely decide anything about one person. Nothing on this page is a diagnosis, and health decisions should be made with a clinician who can see your whole picture.

Where does the information about rs72829446 come from?

GWAS Catalog, Hum Mol Genet 2012, PMID:22936694. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

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