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Exostosis of jaw (PheCode 526.8)

CRYBG1 · rs111829969

Where this position leads

Condition: Exostosis of Jaw

rs111829969 Condition: Exostosis of Jaw Exostosis of Jaw Condition rs111829969 rs111829969 CRYBG1

What the study found

Who was studied 214 African American or Afro-Caribbean cases, 120,940 African American or Afro-Caribbean controls, 451 European ancestry cases, 448,942 European ancestry controls.

The effect Each copy of the C allele shifted the measure 4.83 lower (95% confidence interval 4.83-4.84); p = 2 × 10−11.

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

Where it sits Chromosome 6, band 6q21 — in an intron of CRYBG1.

What each result means

C/C Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Exostosis of jaw (PheCode 526.8) compared to the general population.
C/T Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Exostosis of jaw (PheCode 526.8).
T/T Published research associates this genotype with typical/baseline likelihood of Exostosis of jaw (PheCode 526.8) — no copies of the reported risk allele.
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 rs111829969

What is rs111829969?

rs111829969 is a single position in the genome, in or near the CRYBG1 gene. Published research associates it with exostosis of jaw (phecode 526.8). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs111829969 linked to?

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

Does having rs111829969 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 rs111829969 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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Exostosis of jaw (PheCode 526.8) (rs111829969). MyGeneLog™. https://www.mygenelog.com/variants/rs111829969

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