Standard

Multiple myeloma

near CCDC71L · rs17507636

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 (two copies of the reported risk allele) with a higher likelihood of Multiple myeloma compared to the general population. (GWAS Catalog, Nat Commun 2018, PMID:30213928)

C/T Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Multiple myeloma. (GWAS Catalog, Nat Commun 2018, PMID:30213928)

T/T Published research associates this genotype with typical/baseline likelihood of Multiple myeloma — no copies of the reported risk allele. (GWAS Catalog, Nat Commun 2018, PMID:30213928)

Source: GWAS Catalog, Nat Commun 2018, PMID:30213928

Questions about rs17507636

What is rs17507636?

rs17507636 is a single position in the genome, in or near the near CCDC71L gene. Published research associates it with multiple myeloma. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs17507636 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 rs17507636 come from?

GWAS Catalog, Nat Commun 2018, PMID:30213928. 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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