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Open-angle glaucoma (PheCode 365.1)

BNC2 · rs2149157

Where this position leads

Condition: Glaucoma

rs2149157 Condition: Glaucoma Glaucoma Condition rs2149157 rs2149157 BNC2

What the study found

Who was studied 30,309 African American or Afro-Caribbean cases, 84,722 African American or Afro-Caribbean controls, 8,523 Hispanic or Latin American cases, 48,779 Hispanic or Latin American controls, 1,127 East Asian ancestry cases, 5,402 East Asian ancestry controls, 56,207 European ancestry cases, 377,826 European ancestry controls.

The effect Each copy of the T allele shifted the measure 0.0601 higher (95% confidence interval 0.046-0.074); p = 7 × 10−18.

How common The T allele had a frequency of about 68% in the people studied.

Where it sits Chromosome 9, band 9p22.3 — in an intron of BNC2.

What each result means

C/C No copy of the version the research linked to Open-angle glaucoma (PheCode 365.1). This is the starting point the study compared everyone against.
C/T One copy of the version the research linked to Open-angle glaucoma (PheCode 365.1). That is a smaller link than two copies.
T/T Two copies of the version the research linked to Open-angle glaucoma (PheCode 365.1). 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 rs2149157

What is rs2149157?

rs2149157 is a single position in the genome, in or near the BNC2 gene. Published research associates it with open-angle glaucoma (phecode 365.1). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs2149157 linked to?

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

Does having rs2149157 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 rs2149157 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

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Open-angle glaucoma (PheCode 365.1) (rs2149157). MyGeneLog™. https://www.mygenelog.com/variants/rs2149157

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