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ICD10 N87: Dysplasia of cervix uteri

PAX8-AS1 · rs11123172

What the study found

Who was studied 21,126 European ancestry cases, 206,472 European ancestry controls.

The effect Each copy of the T allele carried 1.07 times the odds of ICD10 N87: Dysplasia of cervix uteri (95% confidence interval 1.05-1.09); p = 2 × 10−10.

Where it sits Chromosome 2, band 2q14.1 — in an intron of PAX8-AS1.

What each result means

C/C No copy of the version the research linked to ICD10 N87: Dysplasia of cervix uteri. This is the starting point the study compared everyone against.
C/T One copy of the version the research linked to ICD10 N87: Dysplasia of cervix uteri. That is a smaller link than two copies.
T/T Two copies of the version the research linked to ICD10 N87: Dysplasia of cervix uteri. That is the strongest link of the three results. A link in a study is not a diagnosis.
Source

Questions about rs11123172

What is rs11123172?

rs11123172 is a single position in the genome, in or near the PAX8-AS1 gene. Published research associates it with icd10 n87: dysplasia of cervix uteri. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs11123172 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 rs11123172 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.

Quoting this page

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ICD10 N87: Dysplasia of cervix uteri (rs11123172). MyGeneLog™. https://www.mygenelog.com/variants/rs11123172

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