Standard

Headache

BTN2A2 · rs2072806

Where this position leads

Condition: Headache

rs2072806 Condition: Headache Headache Condition rs2072806 rs2072806 BTN2A2

What the study found

Who was studied 74,461 British ancestry cases, 149,321 British ancestry controls.

The effect Each copy of the G allele shifted the measure 0.0121 lower (95% confidence interval 0.008-0.0162); p = 5 × 10−9.

Where it sits Chromosome 6, band 6p22.2 — in an intron of BTN2A2.

What each result means

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

Questions about rs2072806

What is rs2072806?

rs2072806 is a single position in the genome, in or near the BTN2A2 gene. Published research associates it with headache. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs2072806 linked to?

On MyGeneLog this position is linked to Headache. The research behind each link, and its sources, are set out on that condition page.

Does having rs2072806 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 rs2072806 come from?

GWAS Catalog, EBioMedicine 2018, PMID:29397368. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

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