Standard
Chronic lymphocytic leukemia
CAMK2D · rs6858698
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 Chronic lymphocytic leukemia compared to the general population. (GWAS Catalog, Nat Genet 2013, PMID:24292274)
C/G
Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Chronic lymphocytic leukemia. (GWAS Catalog, Nat Genet 2013, PMID:24292274)
G/G
Published research associates this genotype with typical/baseline likelihood of Chronic lymphocytic leukemia — no copies of the reported risk allele. (GWAS Catalog, Nat Genet 2013, PMID:24292274)
Source
A genome-wide association study identifies multiple susceptibility loci for chronic lymphocytic leukemia
Speedy HE,
Di Bernardo MC,
Sava GP,
Dyer MJ,
Holroyd A,
Wang Y,
Sunter NJ,
Mansouri L,
Juliusson G,
Smedby KE,
Roos G,
Jayne S
and 17 more — show all
Majid A,
Dearden C,
Hall AG,
Mainou-Fowler T,
Jackson GH,
Summerfield G,
Harris RJ,
Pettitt AR,
Allsup DJ,
Bailey JR,
Pratt G,
Pepper C,
Fegan C,
Rosenquist R,
Catovsky D,
Allan JM,
Houlston RS
Nature genetics · 2014 · PMID 24292274
Questions about rs6858698
What is rs6858698?
rs6858698 is a single position in the genome, in or near the CAMK2D gene. Published research associates it with chronic lymphocytic leukemia. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs6858698 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 rs6858698 come from?
GWAS Catalog, Nat Genet 2013, PMID:24292274. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
← See all variants