Sensitive

Non-cardia gastric cancer

ASH1L · rs80142782

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 Non-cardia gastric cancer — no copies of the reported risk allele. (GWAS Catalog, Gut 2015, PMID:26701879)

C/T Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Non-cardia gastric cancer. (GWAS Catalog, Gut 2015, PMID:26701879)

T/T Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Non-cardia gastric cancer compared to the general population. (GWAS Catalog, Gut 2015, PMID:26701879)

Source: GWAS Catalog, Gut 2015, PMID:26701879

Questions about rs80142782

What is rs80142782?

rs80142782 is a single position in the genome, in or near the ASH1L gene. Published research associates it with non-cardia gastric cancer. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs80142782 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 rs80142782 come from?

GWAS Catalog, Gut 2015, PMID:26701879. 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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