Standard
Ewing sarcoma
BMF · rs4924410
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 Ewing sarcoma compared to the general population.
A/C
Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Ewing sarcoma.
C/C
Published research associates this genotype with typical/baseline likelihood of Ewing sarcoma — no copies of the reported risk allele.
Source
Common variants near TARDBP and EGR2 are associated with susceptibility to Ewing sarcoma
Postel-Vinay S,
Véron AS,
Tirode F,
Pierron G,
Reynaud S,
Kovar H,
Oberlin O,
Lapouble E,
Ballet S,
Lucchesi C,
Kontny U,
González-Neira A
and 14 more — show all
Picci P,
Alonso J,
Patino-Garcia A,
de Paillerets BB,
Laud K,
Dina C,
Froguel P,
Clavel-Chapelon F,
Doz F,
Michon J,
Chanock SJ,
Thomas G,
Cox DG,
Delattre O
Nature genetics · 2012 · PMID 22327514
Questions about rs4924410
What is rs4924410?
rs4924410 is a single position in the genome, in or near the BMF gene. Published research associates it with ewing sarcoma. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs4924410 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 rs4924410 come from?
GWAS Catalog, Nat Genet 2012, PMID:22327514. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
← See all variants