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Sex hormone levels

FSHB · rs11031005

What each result means

C/C Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Sex hormone levels compared to the general population. (GWAS Catalog, Eur J Hum Genet 2015, PMID:26014426)
C/T Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Sex hormone levels. (GWAS Catalog, Eur J Hum Genet 2015, PMID:26014426)
T/T Published research associates this genotype with typical/baseline likelihood of Sex hormone levels — no copies of the reported risk allele. (GWAS Catalog, Eur J Hum Genet 2015, PMID:26014426)
Source

Questions about rs11031005

What is rs11031005?

rs11031005 is a single position in the genome, in or near the FSHB gene. Published research associates it with sex hormone levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs11031005 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 rs11031005 come from?

GWAS Catalog, Eur J Hum Genet 2015, PMID:26014426. 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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