Standard

Fracture

MBL2 · rs11003047

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

G/G Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Fracture compared to the general population. (GWAS Catalog, BMJ 2018, PMID:30158200)

G/T Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Fracture. (GWAS Catalog, BMJ 2018, PMID:30158200)

T/T Published research associates this genotype with typical/baseline likelihood of Fracture — no copies of the reported risk allele. (GWAS Catalog, BMJ 2018, PMID:30158200)

Source: GWAS Catalog, BMJ 2018, PMID:30158200

Questions about rs11003047

What is rs11003047?

rs11003047 is a single position in the genome, in or near the MBL2 gene. Published research associates it with fracture. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs11003047 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 rs11003047 come from?

GWAS Catalog, BMJ 2018, PMID:30158200. 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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