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Histidine levels

near RPL32P20 · rs11776164

What the study found

Who was studied 4,435 East Asian ancestry individuals, 11,340 South Asian ancestry individuals, 120,241 European ancestry individuals.

The effect Each copy of the T allele shifted the measure 0.0371 lower (95% confidence interval 0.026-0.048); p = 1 × 10−11.

How common The T allele had a frequency of about 84% in the people studied.

Where it sits Chromosome 8, band 8q24.22 — between genes, 5.9 kb from RPL32P20.

What each result means

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

Questions about rs11776164

What is rs11776164?

rs11776164 is a single position in the genome, in or near the near RPL32P20 gene. Published research associates it with histidine levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs11776164 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 rs11776164 come from?

GWAS Catalog, Nature 2024, PMID:38448586. 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.

Histidine levels (rs11776164). MyGeneLog™. https://www.mygenelog.com/variants/rs11776164

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