Standard

Fracture of forearm

SUPT3H · rs3957282

What the study found

Who was studied 50,471 European ancestry cases, 969,623 European ancestry controls; replicated in 49,555 cases, 620,360 controls.

The effect Each copy of the T allele carried 1.08 times the odds of Fracture of forearm (95% confidence interval 1.05-1.11); p = 2 × 10−10.

How common The T allele had a frequency of about 5% in the people studied.

Where it sits Chromosome 6, band 6p21.1 — in an intron of SUPT3H.

What each result means

C/C No copy of the version the research linked to Fracture of forearm. This is the starting point the study compared everyone against.
C/T One copy of the version the research linked to Fracture of forearm. That is a smaller link than two copies.
T/T Two copies of the version the research linked to Fracture of forearm. That is the strongest link of the three results. A link in a study is not a diagnosis.
Source

Questions about rs3957282

What is rs3957282?

rs3957282 is a single position in the genome, in or near the SUPT3H gene. Published research associates it with fracture of forearm. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs3957282 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 rs3957282 come from?

GWAS Catalog, Nature genetics 2023, PMID:37919453. 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.

Fracture of forearm (rs3957282). MyGeneLog™. https://www.mygenelog.com/variants/rs3957282

← See all variants