Standard
Lymphoma
LPXN · rs12289961
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 Lymphoma — no copies of the reported risk allele. (GWAS Catalog, PLoS Genet 2013, PMID:23349640)
C/T
Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Lymphoma. (GWAS Catalog, PLoS Genet 2013, PMID:23349640)
T/T
Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Lymphoma compared to the general population. (GWAS Catalog, PLoS Genet 2013, PMID:23349640)
Source
Susceptibility loci associated with specific and shared subtypes of lymphoid malignancies
Vijai J,
Kirchhoff T,
Schrader KA,
Brown J,
Dutra-Clarke AV,
Manschreck C,
Hansen N,
Rau-Murthy R,
Sarrel K,
Przybylo J,
Shah S,
Cheguri S
and 13 more — show all
Stadler Z,
Zhang L,
Paltiel O,
Ben-Yehuda D,
Viale A,
Portlock C,
Straus D,
Lipkin SM,
Lacher M,
Robson M,
Klein RJ,
Zelenetz A,
Offit K
PLoS genetics · 2013 · PMID 23349640 · open access
Questions about rs12289961
What is rs12289961?
rs12289961 is a single position in the genome, in or near the LPXN gene. Published research associates it with lymphoma. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs12289961 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 rs12289961 come from?
GWAS Catalog, PLoS Genet 2013, PMID:23349640. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
← See all variants