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Back pain

DCC · rs7226995

Strength of the evidence

1 / 4

Its strongest genetic-study result is p = 10−8, with 1 associations in the GWAS Catalog.

How this is scored

4: ClinVar disease-causing, reviewed by an expert panel or a guideline (3–4 stars). 3: ClinVar, several labs agreeing (2 stars), or a genetic study at p ≤ 10−50. 2: ClinVar from one lab (1 star), or p ≤ 10−20. 1: ClinVar submitted without criteria (0 stars), or genome-wide significance (p ≤ 5×10−8). The higher of the two counts. It says how solid the evidence is, not whether it matters for a particular person.

What the study found

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

The effect Each copy of the A allele shifted the measure 0.0273 lower (95% confidence interval 0.018-0.037); p = 1 × 10−8.

How common The A allele had a frequency of about 47% in the people studied.

Where it sits Chromosome 18, band 18q21.2 — in an intron of DCC.

What each result means

A/A 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.
A/G One copy of the version the research linked to Back pain. That is a smaller link than two copies.
G/G No copy of the version the research linked to Back pain. This is the starting point the study compared everyone against.
Source

Questions about rs7226995

What is rs7226995?

rs7226995 is a single position in the genome, in or near the DCC 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 rs7226995 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 rs7226995 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 (rs7226995). MyGeneLog™. https://www.mygenelog.com/variants/rs7226995

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