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Female infertility (idiopathic, defined by coding in electronic health record)

near MIR3937 · rs192462512

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 10,872 European and South Asian ancestry female cases, 694,433 European and South Asian ancestry female controls.

The effect Each copy of the C allele carried 0.23 times the odds of Female infertility (idiopathic, defined by coding in electronic health record) (95% confidence interval 0.142-0.363); p = 5 × 10−10.

How common The C allele had a frequency of about 0% in the people studied.

Where it sits Chromosome X, band Xp11.4 — between genes, 7.5 kb from MIR3937.

What each result means

C/C Two copies of the version the research linked to Female infertility (idiopathic, defined by coding in electronic health record). That is the strongest link of the three results. A link in a study is not a diagnosis.
C/T One copy of the version the research linked to Female infertility (idiopathic, defined by coding in electronic health record). That is a smaller link than two copies.
T/T No copy of the version the research linked to Female infertility (idiopathic, defined by coding in electronic health record). This is the starting point the study compared everyone against.
Source
Genome-wide analyses identify 25 infertility loci and relationships with reproductive traits across the allele frequency spectrum
Venkatesh SS, Wittemans LBL, Palmer DS, Baya NA, Ferreira T, Hill B, Lassen FH, Parker MJ, Reibe S, Elhakeem A, Banasik K, Bruun MT
and 39 more — show all
Erikstrup C, Aagard Jensen B, Juul A, Mikkelsen C, Nielsen HS, Ostrowski SR, Pedersen OB, Rohde PD, Sørensen E, Ullum H, Westergaard D, Haraldsson A, Holm H, Jonsdottir I, Olafsson I, Steingrimsdottir T, Steinthorsdottir V, Thorleifsson G, Figueredo J, Karjalainen MK, Pasanen A, Jacobs BM, Kalantzis G, Hubers N, Lippincott M, Fraser A, Lawlor DA, Timpson NJ, Nyegaard M, Stefansson K, Magi R, Laivuori H, van Heel DA, Boomsma DI, Balasubramanian R, Seminara SB, Chan YM, Laisk T, Lindgren CM
Genes & Health Research Team · Estonian Biobank Research Team · Estonian Health Informatics Research Team · DBDS Genomic Consortium · FinnGen
Nature genetics · 2025 · PMID 40229599 · open access

Questions about rs192462512

What is rs192462512?

rs192462512 is a single position in the genome, in or near the near MIR3937 gene. Published research associates it with female infertility (idiopathic, defined by coding in electronic health record). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs192462512 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 rs192462512 come from?

GWAS Catalog, Nature genetics 2025, PMID:40229599. 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.

Female infertility (idiopathic, defined by coding in electronic health record) (rs192462512). MyGeneLog™. https://www.mygenelog.com/variants/rs192462512

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