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Homocysteine levels

CPS1 · rs7422339

No connections yet. This position is published on its own. When a condition, drug or sense page here covers it, the links appear on this page automatically.

What each result means

A/A Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Homocysteine levels compared to the general population. (GWAS Catalog, Hum Mol Genet 2010, PMID:20154341)
A/C Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Homocysteine levels. (GWAS Catalog, Hum Mol Genet 2010, PMID:20154341)
C/C Published research associates this genotype with typical/baseline likelihood of Homocysteine levels — no copies of the reported risk allele. (GWAS Catalog, Hum Mol Genet 2010, PMID:20154341)

Source: GWAS Catalog, Hum Mol Genet 2010, PMID:20154341

Questions about rs7422339

What is rs7422339?

rs7422339 is a single position in the genome, in or near the CPS1 gene. Published research associates it with homocysteine levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs7422339 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 rs7422339 come from?

GWAS Catalog, Hum Mol Genet 2010, PMID:20154341. 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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