ZFAT · rs72609897
Where this position leads
Condition: Hip Circumference
Strength of the evidence
Its strongest genetic-study result is p = 10−8, with 3 associations in the GWAS Catalog.
4: ClinVar disease-causing, reviewed by an expert panel or a guideline (3–4 stars). 3: ClinVar, several labs agreeing (2 stars), or a genetic study at p ≤ 10−50. 2: ClinVar from one lab (1 star), or p ≤ 10−20. 1: ClinVar submitted without criteria (0 stars), or genome-wide significance (p ≤ 5×10−8). The higher of the two counts. It says how solid the evidence is, not whether it matters for a particular person.
What the study found
Who was studied 219,872 British ancestry women.
The effect Each copy of the G allele shifted the measure 0.0206 lower (95% confidence interval 0.014-0.028); p = 1 × 10−8.
Where it sits Chromosome 8, band 8q24.22 — in an intron of ZFAT.
How common each version is
AG
A 62.2% · G 37.8%
A 60.7% · G 39.3%
A 61.4% · G 38.6%
A 66.0% · G 34.0%
A 59.9% · G 40.1%
A 84.5% · G 15.4%
A 79.8% · G 20.2%
A 85.0% · G 15.0%
The share of all copies of this position that are each version. Source: the population studies published in dbSNP (US NCBI); each row names its study.
rs72609897 is a single position in the genome, in or near the ZFAT gene. Published research associates it with hip circumference adjusted for bmi. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
On MyGeneLog this position is linked to Hip Circumference. The research behind each link, and its sources, are set out on that condition page.
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.
GWAS Catalog, Scientific reports 2021, PMID:34021172. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
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Hip circumference adjusted for BMI (rs72609897). MyGeneLog™. https://www.mygenelog.com/variants/rs72609897