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Complex regional/central pain syndrome (PheCode 355)

near RN7SL679P · rs535285063

Where this position leads

Condition: Complex Regional/central Pain Syndrome

rs535285063 Condition: Complex Regional/central Pain Syndrome Complex Regional/central Pain Syndrome Condition rs535285063 rs535285063 near RN7SL67…

What the study found

Who was studied 555 African American or Afro-Caribbean cases, 120,489 African American or Afro-Caribbean controls, 2,258 European ancestry cases, 445,486 European ancestry controls, 309 Hispanic or Latin American cases, 59,203 Hispanic or Latin American controls.

The effect Each copy of the G allele shifted the measure 1.67 lower (95% confidence interval 1.6-1.74); p = 4 × 10−11.

How common The G allele had a frequency of about 100% in the people studied.

Where it sits Chromosome 1, band 1p36.11 — between genes, 7.3 kb from RN7SL679P.

What each result means

A/A No copy of the version the research linked to Complex regional/central pain syndrome (PheCode 355). This is the starting point the study compared everyone against.
A/G One copy of the version the research linked to Complex regional/central pain syndrome (PheCode 355). That is a smaller link than two copies.
G/G Two copies of the version the research linked to Complex regional/central pain syndrome (PheCode 355). That is the strongest link of the three results. A link in a study is not a diagnosis.
Source
Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program
Verma A, Huffman JE, Rodriguez A, Conery M, Liu M, Ho YL, Kim Y, Heise DA, Guare L, Panickan VA, Garcon H, Linares F
and 59 more — show all
Costa L, Goethert I, Tipton R, Honerlaw J, Davies L, Whitbourne S, Cohen J, Posner DC, Sangar R, Murray M, Wang X, Dochtermann DR, Devineni P, Shi Y, Nandi TN, Assimes TL, Brunette CA, Carroll RJ, Clifford R, Duvall S, Gelernter J, Hung A, Iyengar SK, Joseph J, Kember R, Kranzler H, Kripke CM, Levey D, Luoh SW, Merritt VC, Overstreet C, Deak JD, Grant SFA, Polimanti R, Roussos P, Shakt G, Sun YV, Tsao N, Venkatesh S, Voloudakis G, Justice A, Begoli E, Ramoni R, Tourassi G, Pyarajan S, Tsao P, O'Donnell CJ, Muralidhar S, Moser J, Casas JP, Bick AG, Zhou W, Cai T, Voight BF, Cho K, Gaziano JM, Madduri RK, Damrauer S, Liao KP
Science (New York, N.Y.) · 2024 · PMID 39024449 · open access

Questions about rs535285063

What is rs535285063?

rs535285063 is a single position in the genome, in or near the near RN7SL679P gene. Published research associates it with complex regional/central pain syndrome (phecode 355). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs535285063 linked to?

On MyGeneLog this position is linked to Complex Regional/central Pain Syndrome. The research behind each link, and its sources, are set out on that condition page.

Does having rs535285063 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 rs535285063 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.

Complex regional/central pain syndrome (PheCode 355) (rs535285063). MyGeneLog™. https://www.mygenelog.com/variants/rs535285063

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