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What is your height? (cm, inv-normal transformed)

NFATC4 · rs11628929

Where this position leads

Condition: Height

rs11628929 Condition: Height Height Condition rs11628929 rs11628929 NFATC4

What the study found

Who was studied 51,137 African American or Afro-Caribbean individuals, 27,055 Hispanic or Latin American individuals, 3,110 East Asian ancestry individuals, 283,251 European ancestry individuals.

The effect Each copy of the A allele shifted the measure 0.0378 higher (95% confidence interval 0.03-0.046); p = 1 × 10−19.

How common The A allele had a frequency of about 41% in the people studied.

Where it sits Chromosome 14, band 14q12 — in an intron of NFATC4.

What each result means

A/A Two copies of the version the research linked to What is your height? (cm, inv-normal transformed). 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 What is your height? (cm, inv-normal transformed). That is a smaller link than two copies.
G/G No copy of the version the research linked to What is your height? (cm, inv-normal transformed). This is the starting point the study compared everyone against.
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 rs11628929

What is rs11628929?

rs11628929 is a single position in the genome, in or near the NFATC4 gene. Published research associates it with what is your height? (cm, inv-normal transformed). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs11628929 linked to?

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

Does having rs11628929 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 rs11628929 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.

What is your height? (cm, inv-normal transformed) (rs11628929). MyGeneLog™. https://www.mygenelog.com/variants/rs11628929

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