Sensitive

Peyronie's disease (PheCode 604.3)

near RN7SL636P · rs1040551

Where this position leads

Condition: Peyronie's Disease

rs1040551 Condition: Peyronie's Disease Peyronie's Disease Condition rs1040551 rs1040551 near RN7SL63…

What the study found

Who was studied 412 African American or Afro-Caribbean cases, 104,388 African American or Afro-Caribbean controls, 2,512 European ancestry cases, 413,591 European ancestry controls, 275 Hispanic or Latin American cases, 53,398 Hispanic or Latin American controls.

The effect Each copy of the G allele shifted the measure 0.191 lower (95% confidence interval 0.15-0.23); p = 5 × 10−13.

How common The G allele had a frequency of about 54% in the people studied.

Where it sits Chromosome 20, band 20q13.13 — between genes, 15.9 kb from RN7SL636P.

What each result means

G/G Two copies of the version the research linked to Peyronie's disease (PheCode 604.3). That is the strongest link of the three results. A link in a study is not a diagnosis.
G/T One copy of the version the research linked to Peyronie's disease (PheCode 604.3). That is a smaller link than two copies.
T/T No copy of the version the research linked to Peyronie's disease (PheCode 604.3). This is the starting point the study compared everyone against.
Source

Questions about rs1040551

What is rs1040551?

rs1040551 is a single position in the genome, in or near the near RN7SL636P gene. Published research associates it with peyronie's disease (phecode 604.3). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs1040551 linked to?

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

Does having rs1040551 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 rs1040551 come from?

GWAS Catalog, Science (New York, N.Y.) 2024, PMID:39024449. 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.

Peyronie's disease (PheCode 604.3) (rs1040551). MyGeneLog™. https://www.mygenelog.com/variants/rs1040551

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