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White blood cell types

HBS1L · rs9373124

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 White blood cell types — no copies of the reported risk allele. (GWAS Catalog, PLoS Genet 2011, PMID:21738478)

C/T Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with White blood cell types. (GWAS Catalog, PLoS Genet 2011, PMID:21738478)

T/T Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of White blood cell types compared to the general population. (GWAS Catalog, PLoS Genet 2011, PMID:21738478)

Source: GWAS Catalog, PLoS Genet 2011, PMID:21738478

Questions about rs9373124

What is rs9373124?

rs9373124 is a single position in the genome, in or near the HBS1L gene. Published research associates it with white blood cell types. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs9373124 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 rs9373124 come from?

GWAS Catalog, PLoS Genet 2011, PMID:21738478. 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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