Sensitive
Esophageal cancer
ANP32A · rs8030672
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 Esophageal cancer compared to the general population.
A/T
Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Esophageal cancer.
T/T
Published research associates this genotype with typical/baseline likelihood of Esophageal cancer — no copies of the reported risk allele.
Source
Genome-wide association study identifies three new susceptibility loci for esophageal squamous-cell carcinoma in Chinese populations
Wu C,
Hu Z,
He Z,
Jia W,
Wang F,
Zhou Y,
Liu Z,
Zhan Q,
Liu Y,
Yu D,
Zhai K,
Chang J
and 13 more — show all
Qiao Y,
Jin G,
Liu Z,
Shen Y,
Guo C,
Fu J,
Miao X,
Tan W,
Shen H,
Ke Y,
Zeng Y,
Wu T,
Lin D
Nature genetics · 2011 · PMID 21642993
Questions about rs8030672
What is rs8030672?
rs8030672 is a single position in the genome, in or near the ANP32A gene. Published research associates it with esophageal cancer. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs8030672 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 rs8030672 come from?
GWAS Catalog, Nat Genet 2011, PMID:21642993. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
← See all variants