Standard

Diastolic blood pressure

near GUCY1A1 · rs7436887

Where this position leads

Condition: Blood Pressure

rs7436887 Condition: Blood Pressure Blood Pressure Condition rs7436887 rs7436887 near GUCY1A1

What the study found

Who was studied 130,777 Japanese ancestry individuals; replicated in 53,008 East Asian individuals, 105,253 European ancestry individuals.

The effect Each copy of the A allele shifted the measure 0.255 higher (95% confidence interval 0.17-0.34); p = 9 × 10−10.

How common The A allele had a frequency of about 66% in the people studied.

Where it sits Chromosome 4, band 4q32.1 — between genes, 6.4 kb from LOC105377504.

What each result means

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

Questions about rs7436887

What is rs7436887?

rs7436887 is a single position in the genome, in or near the near GUCY1A1 gene. Published research associates it with diastolic blood pressure. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs7436887 linked to?

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

Does having rs7436887 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 rs7436887 come from?

GWAS Catalog, Nat Commun 2018, PMID:30487518. 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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