Standard
Follicular lymphoma
PVT1 · rs13254990
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 Follicular lymphoma — no copies of the reported risk allele.
C/T
Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Follicular lymphoma.
T/T
Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Follicular lymphoma compared to the general population.
Source
Genome-wide association study identifies five susceptibility loci for follicular lymphoma outside the HLA region
Skibola CF,
Berndt SI,
Vijai J,
Conde L,
Wang Z,
Yeager M,
de Bakker PI,
Birmann BM,
Vajdic CM,
Foo JN,
Bracci PM,
Vermeulen RC
and 100 more — show all
Slager SL,
de Sanjose S,
Wang SS,
Linet MS,
Salles G,
Lan Q,
Severi G,
Hjalgrim H,
Lightfoot T,
Melbye M,
Gu J,
Ghesquières H,
Link BK,
Morton LM,
Holly EA,
Smith A,
Tinker LF,
Teras LR,
Kricker A,
Becker N,
Purdue MP,
Spinelli JJ,
Zhang Y,
Giles GG,
Vineis P,
Monnereau A,
Bertrand KA,
Albanes D,
Zeleniuch-Jacquotte A,
Gabbas A,
Chung CC,
Burdett L,
Hutchinson A,
Lawrence C,
Montalvan R,
Liang L,
Huang J,
Ma B,
Liu J,
Adami HO,
Glimelius B,
Ye Y,
Nowakowski GS,
Dogan A,
Thompson CA,
Habermann TM,
Novak AJ,
Liebow M,
Witzig TE,
Weiner GJ,
Schenk M,
Hartge P,
De Roos AJ,
Cozen W,
Zhi D,
Akers NK,
Riby J,
Smith MT,
Lacher M,
Villano DJ,
Maria A,
Roman E,
Kane E,
Jackson RD,
North KE,
Diver WR,
Turner J,
Armstrong BK,
Benavente Y,
Boffetta P,
Brennan P,
Foretova L,
Maynadie M,
Staines A,
McKay J,
Brooks-Wilson AR,
Zheng T,
Holford TR,
Chamosa S,
Kaaks R,
Kelly RS,
Ohlsson B,
Travis RC,
Weiderpass E,
Clavel J,
Giovannucci E,
Kraft P,
Virtamo J,
Mazza P,
Cocco P,
Ennas MG,
Chiu BC,
Fraumeni JF Jr,
Nieters A,
Offit K,
Wu X,
Cerhan JR,
Smedby KE,
Chanock SJ,
Rothman N
American journal of human genetics · 2014 · PMID 25279986
What people read about alongside this
Papers in Europe PMC whose title or abstract names both this rsID and that subject. A shared paper means somebody wrote about the two together — it is not a claim that this position explains the subject.
Questions about rs13254990
What is rs13254990?
rs13254990 is a single position in the genome, in or near the PVT1 gene. Published research associates it with follicular lymphoma. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What do people read about alongside rs13254990?
Subjects that appear in the title or abstract of the same papers as this rsID include infection and immunity (1 papers). A shared paper means somebody wrote about the two together; it is not a claim that this position explains the topic.
Does having rs13254990 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 rs13254990 come from?
GWAS Catalog, Am J Hum Genet 2014, PMID:25279986. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
← See all variants