Standard
Urinary metabolites (H-NMR features)
ALMS1 · rs11884776
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 Urinary metabolites (H-NMR features) compared to the general population. (GWAS Catalog, PLoS Genet 2014, PMID:24586186)
C/T
Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Urinary metabolites (H-NMR features). (GWAS Catalog, PLoS Genet 2014, PMID:24586186)
T/T
Published research associates this genotype with typical/baseline likelihood of Urinary metabolites (H-NMR features) — no copies of the reported risk allele. (GWAS Catalog, PLoS Genet 2014, PMID:24586186)
Source
Genome-wide association study of metabolic traits reveals novel gene-metabolite-disease links
Rueedi R,
Ledda M,
Nicholls AW,
Salek RM,
Marques-Vidal P,
Morya E,
Sameshima K,
Montoliu I,
Da Silva L,
Collino S,
Martin FP,
Rezzi S
and 10 more — show all
PLoS genetics · 2014 · PMID 24586186 · open access
Questions about rs11884776
What is rs11884776?
rs11884776 is a single position in the genome, in or near the ALMS1 gene. Published research associates it with urinary metabolites (h-nmr features). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs11884776 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 rs11884776 come from?
GWAS Catalog, PLoS Genet 2014, PMID:24586186. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
← See all variants