Standard

Hearing function

SIK3 · rs681524

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 Hearing function compared to the general population.

C/T Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Hearing function.

T/T Published research associates this genotype with typical/baseline likelihood of Hearing function — no copies of the reported risk allele.

Source

Salt-inducible kinase 3, SIK3, is a new gene associated with hearing

Wolber LE, Girotto G, Buniello A, Vuckovic D, Pirastu N, Lorente-Cánovas B, Rudan I, Hayward C, Polasek O, Ciullo M, Mangino M, Steves C

and 6 more — show all

Concas MP, Cocca M, Spector TD, Gasparini P, Steel KP, Williams FM

Human molecular genetics · 2014 · PMID 25060954 · open access

Questions about rs681524

What is rs681524?

rs681524 is a single position in the genome, in or near the SIK3 gene. Published research associates it with hearing function. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs681524 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 rs681524 come from?

GWAS Catalog, Hum Mol Genet 2014, PMID:25060954. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

← See all variants