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Stands on its own.
Nothing else here links to this position yet — but the page above is the point: what the
research found, what each genotype means, and where it came from, in language you can
read. Links to conditions, drugs and the senses appear automatically if we write them.
What the study found
Who was studied 51,378 European ancestry cases, 243,913 European ancestry controls.
The effect
Each copy of the A allele carried 0.95 times the odds of ICD10 D25: Leiomyoma of uterus (95% confidence interval 0.93-0.96); p = 1 × 10−10.
Where it sits Chromosome 7, band 7q31.31 — in an intron of TSPAN12.
What each result means
A/ATwo copies of the version the research linked to ICD10 D25: Leiomyoma of uterus. That is the strongest link of the three results. A link in a study is not a diagnosis.
A/GOne copy of the version the research linked to ICD10 D25: Leiomyoma of uterus. That is a smaller link than two copies.
G/GNo copy of the version the research linked to ICD10 D25: Leiomyoma of uterus. This is the starting point the study compared everyone against.
rs67679138 is a single position in the genome, in or near the TSPAN12 gene. Published research associates it with icd10 d25: leiomyoma of uterus. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs67679138 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 rs67679138 come from?
GWAS Catalog, Nature medicine 2025, PMID:40069456. 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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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.
ICD10 D25: Leiomyoma of uterus (rs67679138). MyGeneLog™. https://www.mygenelog.com/variants/rs67679138