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CD80 on myeloid Dendritic Cell

BACH2 · rs2325259

What the study found

Who was studied 2,871 Sardinian (founder/genetic isolate) ancestry individuals.

The effect Each copy of the C allele shifted the measure 0.2 higher (95% confidence interval 0.14-0.25); p = 1 × 10−12.

How common The C allele had a frequency of about 44% in the people studied.

Where it sits Chromosome 6, band 6q15 — in an intron of BACH2.

What each result means

C/C Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of CD80 on myeloid Dendritic Cell compared to the general population.
C/T Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with CD80 on myeloid Dendritic Cell.
T/T Published research associates this genotype with typical/baseline likelihood of CD80 on myeloid Dendritic Cell — no copies of the reported risk allele.
Source

Questions about rs2325259

What is rs2325259?

rs2325259 is a single position in the genome, in or near the BACH2 gene. Published research associates it with cd80 on myeloid dendritic cell. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs2325259 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 rs2325259 come from?

GWAS Catalog, Nature genetics 2020, PMID:32929287. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

Quoting this page

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CD80 on myeloid Dendritic Cell (rs2325259). MyGeneLog™. https://www.mygenelog.com/variants/rs2325259

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