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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 2,401 European ancestry cases, 29,182 European ancestry controls.
The effect
The reported allele is T; the catalogue records no effect size
; p = 4 × 10−10.
How common The T allele had a frequency of about 36% in the people studied.
Where it sits Chromosome X, band Xq23 — between genes, 39.8 kb from M6PRP1.
What each result means
C/CNo copy of the version the research linked to Neonatal jaundice (maternal effect). This is the starting point the study compared everyone against.
C/TOne copy of the version the research linked to Neonatal jaundice (maternal effect). That is a smaller link than two copies.
T/TTwo copies of the version the research linked to Neonatal jaundice (maternal effect). That is the strongest link of the three results. A link in a study is not a diagnosis.
Nature communications · 2024 · PMID 39214992 · open access
Questions about rs5942980
What is rs5942980?
rs5942980 is a single position in the genome, in or near the near M6PRP1 gene. Published research associates it with neonatal jaundice (maternal effect). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs5942980 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 rs5942980 come from?
GWAS Catalog, Nature communications 2024, PMID:39214992. 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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