Sensitive
Pancreatic cancer
URAD · rs9581943
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 (two copies of the reported risk allele) with a higher likelihood of Pancreatic cancer compared to the general population.
A/G
Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Pancreatic cancer.
G/G
Published research associates this genotype with typical/baseline likelihood of Pancreatic cancer — no copies of the reported risk allele.
Source
Genome-wide association study identifies multiple susceptibility loci for pancreatic cancer
Wolpin BM,
Rizzato C,
Kraft P,
Kooperberg C,
Petersen GM,
Wang Z,
Arslan AA,
Beane-Freeman L,
Bracci PM,
Buring J,
Canzian F,
Duell EJ
and 106 more — show all
Gallinger S,
Giles GG,
Goodman GE,
Goodman PJ,
Jacobs EJ,
Kamineni A,
Klein AP,
Kolonel LN,
Kulke MH,
Li D,
Malats N,
Olson SH,
Risch HA,
Sesso HD,
Visvanathan K,
White E,
Zheng W,
Zheng W,
Abnet CC,
Albanes D,
Andreotti G,
Austin MA,
Barfield R,
Basso D,
Berndt SI,
Boutron-Ruault MC,
Brotzman M,
Büchler MW,
Bueno-de-Mesquita HB,
Bugert P,
Burdette L,
Campa D,
Caporaso NE,
Capurso G,
Chung C,
Cotterchio M,
Costello E,
Elena J,
Funel N,
Gaziano JM,
Giese NA,
Giovannucci EL,
Goggins M,
Gorman MJ,
Gross M,
Haiman CA,
Hassan M,
Helzlsouer KJ,
Henderson BE,
Holly EA,
Hu N,
Hunter DJ,
Innocenti F,
Jenab M,
Kaaks R,
Key TJ,
Khaw KT,
Klein EA,
Kogevinas M,
Krogh V,
Kupcinskas J,
Kurtz RC,
LaCroix A,
Landi MT,
Landi S,
Le Marchand L,
Mambrini A,
Mannisto S,
Milne RL,
Nakamura Y,
Oberg AL,
Owzar K,
Patel AV,
Peeters PH,
Peters U,
Pezzilli R,
Piepoli A,
Porta M,
Real FX,
Riboli E,
Rothman N,
Scarpa A,
Shu XO,
Silverman DT,
Soucek P,
Sund M,
Talar-Wojnarowska R,
Taylor PR,
Theodoropoulos GE,
Thornquist M,
Tjønneland A,
Tobias GS,
Trichopoulos D,
Vodicka P,
Wactawski-Wende J,
Wentzensen N,
Wu C,
Yu H,
Yu K,
Zeleniuch-Jacquotte A,
Hoover R,
Hartge P,
Fuchs C,
Chanock SJ,
Stolzenberg-Solomon RS,
Amundadottir LT
Nature genetics · 2014 · PMID 25086665 · open access
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 rs9581943
What is rs9581943?
rs9581943 is a single position in the genome, in or near the URAD gene. Published research associates it with pancreatic cancer. 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 rs9581943?
Subjects that appear in the title or abstract of the same papers as this rsID include blood sugar and insulin (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 rs9581943 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 rs9581943 come from?
GWAS Catalog, Nat Genet 2014, PMID:25086665. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
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