Standard
Renal function-related traits (BUN)
BCAS3 · rs11868441
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
A/A
Published research associates this genotype with typical/baseline likelihood of Renal function-related traits (BUN) — no copies of the reported risk allele. (GWAS Catalog, Nat Genet 2012, PMID:22797727)
A/G
Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Renal function-related traits (BUN). (GWAS Catalog, Nat Genet 2012, PMID:22797727)
G/G
Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Renal function-related traits (BUN) compared to the general population. (GWAS Catalog, Nat Genet 2012, PMID:22797727)
Source
Meta-analysis identifies multiple loci associated with kidney function-related traits in east Asian populations
Okada Y,
Sim X,
Go MJ,
Wu JY,
Gu D,
Takeuchi F,
Takahashi A,
Maeda S,
Tsunoda T,
Chen P,
Lim SC,
Wong TY
and 34 more — show all
Liu J,
Young TL,
Aung T,
Seielstad M,
Teo YY,
Kim YJ,
Lee JY,
Han BG,
Kang D,
Chen CH,
Tsai FJ,
Chang LC,
Fann SJ,
Mei H,
Rao DC,
Hixson JE,
Chen S,
Katsuya T,
Isono M,
Ogihara T,
Chambers JC,
Zhang W,
Kooner JS,
Albrecht E,
Yamamoto K,
Kubo M,
Nakamura Y,
Kamatani N,
Kato N,
He J,
Chen YT,
Cho YS,
Tai ES,
Tanaka T
Nature genetics · 2012 · PMID 22797727
Questions about rs11868441
What is rs11868441?
rs11868441 is a single position in the genome, in or near the BCAS3 gene. Published research associates it with renal function-related traits (bun). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs11868441 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 rs11868441 come from?
GWAS Catalog, Nat Genet 2012, PMID:22797727. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
← See all variants