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Red blood cell count

CCND2 · rs11611647

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 (two copies of the reported risk allele) with a higher likelihood of Red blood cell count compared to the general population. (GWAS Catalog, Nat Genet 2010, PMID:20139978)

C/T Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Red blood cell count. (GWAS Catalog, Nat Genet 2010, PMID:20139978)

T/T Published research associates this genotype with typical/baseline likelihood of Red blood cell count — no copies of the reported risk allele. (GWAS Catalog, Nat Genet 2010, PMID:20139978)

Source: GWAS Catalog, Nat Genet 2010, PMID:20139978

Questions about rs11611647

What is rs11611647?

rs11611647 is a single position in the genome, in or near the CCND2 gene. Published research associates it with red blood cell count. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs11611647 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 rs11611647 come from?

GWAS Catalog, Nat Genet 2010, PMID:20139978. 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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