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Phosphatidylcholines levels (UKB data field 23437)

RPS16P2 · rs907863

What the study found

Who was studied 88,268 European ancestry individuals.

The effect Each copy of the T allele shifted the measure 0.0339 lower (95% confidence interval 0.025-0.043); p = 2 × 10−13.

How common The T allele had a frequency of about 36% in the people studied.

Where it sits Chromosome 2, band 2p24.1 — in a non-coding transcript of RPS16P2.

What each result means

C/C No copy of the version the research linked to Phosphatidylcholines levels (UKB data field 23437). This is the starting point the study compared everyone against.
C/T One copy of the version the research linked to Phosphatidylcholines levels (UKB data field 23437). That is a smaller link than two copies.
T/T Two copies of the version the research linked to Phosphatidylcholines levels (UKB data field 23437). That is the strongest link of the three results. A link in a study is not a diagnosis.
Source

Questions about rs907863

What is rs907863?

rs907863 is a single position in the genome, in or near the RPS16P2 gene. Published research associates it with phosphatidylcholines levels (ukb data field 23437). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs907863 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 rs907863 come from?

GWAS Catalog, Biological psychiatry 2023, PMID:36764567. 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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Phosphatidylcholines levels (UKB data field 23437) (rs907863). MyGeneLog™. https://www.mygenelog.com/variants/rs907863

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