Standard

Hip shape mode 10

TMTC2 · rs12369671

What the study found

Who was studied 38,175 European ancestry individuals, 5,310 East Asian ancestry individuals.

The effect Each copy of the T allele shifted the measure 0.1 lower (95% confidence interval 0.08-0.12); p = 1 × 10−20.

How common The T allele had a frequency of about 88% in the people studied.

Where it sits Chromosome 12, band 12q21.31 — in an intron of TMTC2.

What each result means

G/G No copy of the version the research linked to Hip shape mode 10. This is the starting point the study compared everyone against.
G/T One copy of the version the research linked to Hip shape mode 10. That is a smaller link than two copies.
T/T Two copies of the version the research linked to Hip shape mode 10. That is the strongest link of the three results. A link in a study is not a diagnosis.
Source

Questions about rs12369671

What is rs12369671?

rs12369671 is a single position in the genome, in or near the TMTC2 gene. Published research associates it with hip shape mode 10. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs12369671 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 rs12369671 come from?

GWAS Catalog, Human molecular genetics 2025, PMID:39574169. 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.

Hip shape mode 10 (rs12369671). MyGeneLog™. https://www.mygenelog.com/variants/rs12369671

← See all variants