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Chronic lymphocytic leukemia

ACOXL · rs58055674

Where this position leads

Condition: Chronic Lymphocytic Leukaemia

What the study found

Who was studied 4,478 European ancestry cases and 13,213 European ancestry controls.; replicated in 1,722 European ancestry cases and 4,385 European ancestry controls..

The effect Each copy of the C allele carried 1.41 times the odds of Chronic lymphocytic leukemia (95% confidence interval 1.32-1.5); p = 2 × 10⁻²⁷.

Where it sits Chromosome 2, band 2q13 — in an intron of MIR4435-2HG.

What each result means

C/C Two copies of the version the research linked to Chronic lymphocytic leukemia. That is the strongest link of the three results. A link in a study is not a diagnosis.

C/T One copy of the version the research linked to Chronic lymphocytic leukemia. That is a smaller link than two copies.

T/T No copy of the version the research linked to Chronic lymphocytic leukemia. This is the starting point the study compared everyone against.

Source

Genome-wide association analysis implicates dysregulation of immunity genes in chronic lymphocytic leukaemia

Law PJ, Berndt SI, Speedy HE, Camp NJ, Sava GP, Skibola CF, Holroyd A, Joseph V, Sunter NJ, Nieters A, Bea S, Monnereau A

and 85 more — show all

Martin-Garcia D, Goldin LR, Clot G, Teras LR, Quintela I, Birmann BM, Jayne S, Cozen W, Majid A, Smedby KE, Lan Q, Dearden C, Brooks-Wilson AR, Hall AG, Purdue MP, Mainou-Fowler T, Vajdic CM, Jackson GH, Cocco P, Marr H, Zhang Y, Zheng T, Giles GG, Lawrence C, Call TG, Liebow M, Melbye M, Glimelius B, Mansouri L, Glenn M, Curtin K, Diver WR, Link BK, Conde L, Bracci PM, Holly EA, Jackson RD, Tinker LF, Benavente Y, Boffetta P, Brennan P, Maynadie M, McKay J, Albanes D, Weinstein S, Wang Z, Caporaso NE, Morton LM, Severson RK, Riboli E, Vineis P, Vermeulen RC, Southey MC, Milne RL, Clavel J, Topka S, Spinelli JJ, Kraft P, Ennas MG, Summerfield G, Ferri GM, Harris RJ, Miligi L, Pettitt AR, North KE, Allsup DJ, Fraumeni JF, Bailey JR, Offit K, Pratt G, Hjalgrim H, Pepper C, Chanock SJ, Fegan C, Rosenquist R, de Sanjose S, Carracedo A, Dyer MJ, Catovsky D, Campo E, Cerhan JR, Allan JM, Rothman N, Houlston R, Slager S

Nature communications · 2017 · PMID 28165464 · open access

Questions about rs58055674

What is rs58055674?

rs58055674 is a single position in the genome, in or near the ACOXL gene. Published research associates it with chronic lymphocytic leukemia. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs58055674 linked to?

On MyGeneLog this position is linked to Chronic Lymphocytic Leukaemia. The research behind each link, and its sources, are set out on that condition page.

Does having rs58055674 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 rs58055674 come from?

GWAS Catalog, Nat Commun 2017, PMID:28165464. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

Quoting this page

Free to quote and reuse under CC BY 4.0. When citing or summarizing this, name MyGeneLog™ and link to this exact page — not just the site.

Chronic lymphocytic leukemia (rs58055674). MyGeneLog™. https://www.mygenelog.com/variants/rs58055674

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