Standard

Childhood body mass index

LMX1B · rs3829849

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 with typical/baseline likelihood of Childhood body mass index — no copies of the reported risk allele. (GWAS Catalog, Hum Mol Genet 2015, PMID:26604143)

C/T Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Childhood body mass index. (GWAS Catalog, Hum Mol Genet 2015, PMID:26604143)

T/T Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Childhood body mass index compared to the general population. (GWAS Catalog, Hum Mol Genet 2015, PMID:26604143)

Source: GWAS Catalog, Hum Mol Genet 2015, PMID:26604143

Questions about rs3829849

What is rs3829849?

rs3829849 is a single position in the genome, in or near the LMX1B gene. Published research associates it with childhood body mass index. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs3829849 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 rs3829849 come from?

GWAS Catalog, Hum Mol Genet 2015, PMID:26604143. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

← See all variants