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ANGI protein level (protein group normalized intensity)

near Y_RNA · rs10142601

What the study found

Who was studied 1,255 European, Hispanic or African ancestry individuals; replicated in 325 Arab, Indian or Filipino ancestry individuals.

The effect Each copy of the G allele shifted the measure 0.377 higher (95% confidence interval 0.29-0.47); p = 8 × 10−16.

How common The G allele had a frequency of about 16% in the people studied.

Where it sits Chromosome 14, band 14q11.2 — between genes, 4.2 kb from Y_RNA.

What each result means

A/A No copy of the version the research linked to ANGI protein level (protein group normalized intensity). This is the starting point the study compared everyone against.
A/G One copy of the version the research linked to ANGI protein level (protein group normalized intensity). That is a smaller link than two copies.
G/G Two copies of the version the research linked to ANGI protein level (protein group normalized intensity). That is the strongest link of the three results. A link in a study is not a diagnosis.
Source

Questions about rs10142601

What is rs10142601?

rs10142601 is a single position in the genome, in or near the near Y_RNA gene. Published research associates it with angi protein level (protein group normalized intensity). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs10142601 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 rs10142601 come from?

GWAS Catalog, Nature genetics 2025, PMID:41310232. 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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ANGI protein level (protein group normalized intensity) (rs10142601). MyGeneLog™. https://www.mygenelog.com/variants/rs10142601

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