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Back pain

near RNU6-273P · rs8022156

What the study found

Who was studied 119,384 European ancestry cases, 334,478 European ancestry controls.

The effect Each copy of the T allele shifted the measure 0.0337 higher (95% confidence interval 0.023-0.044); p = 5 × 10−10.

How common The T allele had a frequency of about 73% in the people studied.

Where it sits Chromosome 14, band 14q13.3 — between genes, 0.6 kb from RNU6-273P.

What each result means

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

Questions about rs8022156

What is rs8022156?

rs8022156 is a single position in the genome, in or near the near RNU6-273P gene. Published research associates it with back pain. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs8022156 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 rs8022156 come from?

GWAS Catalog, Pain 2019, PMID:30747904. 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.

Back pain (rs8022156). MyGeneLog™. https://www.mygenelog.com/variants/rs8022156

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