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Placental weight (fetal genotype, adjusted for sex)

near RPL31P43 · rs1434836

What the study found

Who was studied 65,651 European ancestry individuals.

The effect Each copy of the A allele shifted the measure 0.0359 higher (95% confidence interval 0.025-0.047); p = 1 × 10−10.

How common The A allele had a frequency of about 58% in the people studied.

Where it sits Chromosome 9, band 9q31.2 — between genes, 19.8 kb from RPL31P43.

What each result means

A/A Two copies of the version the research linked to Placental weight (fetal genotype, adjusted for sex). That is the strongest link of the three results. A link in a study is not a diagnosis.
A/G One copy of the version the research linked to Placental weight (fetal genotype, adjusted for sex). That is a smaller link than two copies.
G/G No copy of the version the research linked to Placental weight (fetal genotype, adjusted for sex). This is the starting point the study compared everyone against.
Source

Questions about rs1434836

What is rs1434836?

rs1434836 is a single position in the genome, in or near the near RPL31P43 gene. Published research associates it with placental weight (fetal genotype, adjusted for sex). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs1434836 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 rs1434836 come from?

GWAS Catalog, Nature genetics 2023, PMID:37798380. 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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Placental weight (fetal genotype, adjusted for sex) (rs1434836). MyGeneLog™. https://www.mygenelog.com/variants/rs1434836

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