Standard

Monocyte side fluorescence

near MIR7702 · rs17207270

What the study found

Who was studied 39,586 European ancestry individuals.

The effect Each copy of the A allele shifted the measure 0.0549 SD units lower (95% confidence interval 0.038-0.072); p = 2 × 10−10.

How common The A allele had a frequency of about 22% in the people studied.

Where it sits Chromosome 9, band 9q31.3 — between genes, 82.4 kb from MIR7702.

What each result means

A/A Two copies of the version the research linked to Monocyte side fluorescence. That is the strongest link of the three results. A link in a study is not a diagnosis.
A/G One copy of the version the research linked to Monocyte side fluorescence. That is a smaller link than two copies.
G/G No copy of the version the research linked to Monocyte side fluorescence. This is the starting point the study compared everyone against.
Source

Questions about rs17207270

What is rs17207270?

rs17207270 is a single position in the genome, in or near the near MIR7702 gene. Published research associates it with monocyte side fluorescence. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs17207270 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 rs17207270 come from?

GWAS Catalog, Nature communications 2023, PMID:37596262. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

Quoting this page

Free to quote and reuse under CC BY 4.0. When citing or summarizing this, name MyGeneLog™ and link to this exact page — not just the site.

Monocyte side fluorescence (rs17207270). MyGeneLog™. https://www.mygenelog.com/variants/rs17207270

← See all variants