Standard
Atopic dermatitis
c6orf10 · rs41268896
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 Atopic dermatitis compared to the general population.
A/G
Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Atopic dermatitis.
G/G
Published research associates this genotype with typical/baseline likelihood of Atopic dermatitis — no copies of the reported risk allele.
Source
Genome-wide comparative analysis of atopic dermatitis and psoriasis gives insight into opposing genetic mechanisms
Baurecht H,
Hotze M,
Brand S,
Büning C,
Cormican P,
Corvin A,
Ellinghaus D,
Ellinghaus E,
Esparza-Gordillo J,
Fölster-Holst R,
Franke A,
Gieger C
and 26 more — show all
Hubner N,
Illig T,
Irvine AD,
Kabesch M,
Lee YA,
Lieb W,
Marenholz I,
McLean WH,
Morris DW,
Mrowietz U,
Nair R,
Nöthen MM,
Novak N,
O'Regan GM,
Schreiber S,
Smith C,
Strauch K,
Stuart PE,
Trembath R,
Tsoi LC,
Weichenthal M,
Barker J,
Elder JT,
Weidinger S,
Cordell HJ,
Brown SJ
American journal of human genetics · 2015 · PMID 25574825 · open access
Questions about rs41268896
What is rs41268896?
rs41268896 is a single position in the genome, in or near the c6orf10 gene. Published research associates it with atopic dermatitis. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs41268896 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 rs41268896 come from?
GWAS Catalog, Am J Hum Genet 2015, PMID:25574825. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
← See all variants