Standard

IgG levels

TNFRSF13B · rs4792800

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 IgG levels — 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 IgG levels.

G/G Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of IgG levels compared to the general population.

Source

Genome-wide association study identifies common variants at TNFRSF13B associated with IgG level in a healthy Chinese male population

Liao M, Ye F, Zhang B, Huang L, Xiao Q, Qin M, Mo L, Tan A, Gao Y, Lu Z, Wu C, Zhang Y

and 5 more — show all

Zhang H, Qin X, Hu Y, Yang X, Mo Z

Genes and immunity · 2012 · PMID 22673310

Questions about rs4792800

What is rs4792800?

rs4792800 is a single position in the genome, in or near the TNFRSF13B gene. Published research associates it with igg levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs4792800 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 rs4792800 come from?

GWAS Catalog, Genes Immun 2012, PMID:22673310. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

← See all variants