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Anthropometric traits in newborns

CCNL1 · rs1482853

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 with typical/baseline likelihood of Anthropometric traits in newborns — no copies of the reported risk allele.

A/C Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Anthropometric traits in newborns.

C/C Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Anthropometric traits in newborns compared to the general population.

Source

The chromosome 3q25 genomic region is associated with measures of adiposity in newborns in a multi-ethnic genome-wide association study

Urbanek M, Hayes MG, Armstrong LL, Morrison J, Lowe LP, Badon SE, Scheftner D, Pluzhnikov A, Levine D, Laurie CC, McHugh C, Ackerman CM

and 9 more — show all

Mirel DB, Doheny KF, Guo C, Scholtens DM, Dyer AR, Metzger BE, Reddy TE, Cox NJ, Lowe WL Jr

HAPO Study Cooperative Research Group

Human molecular genetics · 2013 · PMID 23575227

Questions about rs1482853

What is rs1482853?

rs1482853 is a single position in the genome, in or near the CCNL1 gene. Published research associates it with anthropometric traits in newborns. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs1482853 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 rs1482853 come from?

GWAS Catalog, Hum Mol Genet 2013, PMID:23575227. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

← See all variants