Standard

Smoking initiation

LOC102724623 · rs12545053

What the study found

Who was studied 842,717 European ancestry individuals.

The effect Each copy of the G allele carried 1.02 times the odds of Smoking initiation; p = 4 × 10−10.

Where it sits Chromosome 8, band 8q12.3 — in an intron of LINC01414.

What each result means

A/A Published research associates this genotype with typical/baseline likelihood of Smoking initiation — no copies of the reported risk allele.
A/G Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Smoking initiation.
G/G Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Smoking initiation compared to the general population.
Source

Questions about rs12545053

What is rs12545053?

rs12545053 is a single position in the genome, in or near the LOC102724623 gene. Published research associates it with smoking initiation. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs12545053 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 rs12545053 come from?

GWAS Catalog, Nature communications 2020, PMID:33082346. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

Quoting this page

Free to quote and reuse under CC BY 4.0. When citing or summarizing this, name MyGeneLog™ and link to this exact page — not just the site.

Smoking initiation (rs12545053). MyGeneLog™. https://www.mygenelog.com/variants/rs12545053

← See all variants