Standard
Acne (severe)
SELL · rs7531806
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 Acne (severe) compared to the general population. (GWAS Catalog, Nat Commun 2014, PMID:24399259)
A/G
Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Acne (severe). (GWAS Catalog, Nat Commun 2014, PMID:24399259)
G/G
Published research associates this genotype with typical/baseline likelihood of Acne (severe) — no copies of the reported risk allele. (GWAS Catalog, Nat Commun 2014, PMID:24399259)
Source
Two new susceptibility loci 1q24.2 and 11p11.2 confer risk to severe acne
He L,
Wu WJ,
Yang JK,
Cheng H,
Zuo XB,
Lai W,
Gao TW,
Ma CL,
Luo N,
Huang JQ,
Lu FY,
Liu YQ
and 22 more — show all
Huang YJ,
Lu QJ,
Zhang HL,
Wang L,
Wang WZ,
Wang MM,
Xiao SX,
Sun Q,
Li CY,
Bai YP,
Li H,
Zhou ZC,
Zhou FS,
Chen G,
Liang B,
Qi J,
Yang XY,
Yang T,
Zheng X,
Sun LD,
Zhang XJ,
Zhang YP
Nature communications · 2014 · PMID 24399259
Questions about rs7531806
What is rs7531806?
rs7531806 is a single position in the genome, in or near the SELL gene. Published research associates it with acne (severe). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs7531806 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 rs7531806 come from?
GWAS Catalog, Nat Commun 2014, PMID:24399259. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
← See all variants