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Severe gingival inflammation

ACCN1 · rs11652874

Stands on its own. Nothing else here links to this position yet — but the page above is the point: what the research found, what each genotype means, and where it came from, in language you can read. Links to conditions, drugs and the senses appear automatically if we write them.

What each result means

C/C Published research associates this genotype with typical/baseline likelihood of Severe gingival inflammation — no copies of the reported risk allele. (GWAS Catalog, JDR Clin Trans Res 2016, PMID:28459102)

C/G Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Severe gingival inflammation. (GWAS Catalog, JDR Clin Trans Res 2016, PMID:28459102)

G/G Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Severe gingival inflammation compared to the general population. (GWAS Catalog, JDR Clin Trans Res 2016, PMID:28459102)

Source: GWAS Catalog, JDR Clin Trans Res 2016, PMID:28459102

Questions about rs11652874

What is rs11652874?

rs11652874 is a single position in the genome, in or near the ACCN1 gene. Published research associates it with severe gingival inflammation. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs11652874 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 rs11652874 come from?

GWAS Catalog, JDR Clin Trans Res 2016, PMID:28459102. 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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