Standard

Plasma free amino acid levels (adjusted for twenty other PFAAs)

PSPHL · rs6966061

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 1,338 Japanese ancestry individuals.

The effect Each copy of the A allele shifted the measure 0.18 lower (95% confidence interval 0.14-0.22); p = 9 × 10⁻¹³.

Where it sits Chromosome 7, band 7p11.2 — between genes, 7.8 kb from PSPHP1.

What each result means

A/A Two copies of the version the research linked to Plasma free amino acid levels (adjusted for twenty other PFAAs). 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 Plasma free amino acid levels (adjusted for twenty other PFAAs). That is a smaller link than two copies.

G/G No copy of the version the research linked to Plasma free amino acid levels (adjusted for twenty other PFAAs). This is the starting point the study compared everyone against.

Source

Genetic basis for plasma amino acid concentrations based on absolute quantification: a genome-wide association study in the Japanese population

Imaizumi A, Adachi Y, Kawaguchi T, Higasa K, Tabara Y, Sonomura K, Sato TA, Takahashi M, Mizukoshi T, Yoshida HO, Kageyama N, Okamoto C

and 7 more — show all

Takasu M, Mori M, Noguchi Y, Shimba N, Miyano H, Yamada R, Matsuda F

European journal of human genetics : EJHG · 2019 · PMID 30659259 · open access

Questions about rs6966061

What is rs6966061?

rs6966061 is a single position in the genome, in or near the PSPHL gene. Published research associates it with plasma free amino acid levels (adjusted for twenty other pfaas). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs6966061 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 rs6966061 come from?

GWAS Catalog, European journal of human genetics : EJHG 2019, PMID:30659259. 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.

Plasma free amino acid levels (adjusted for twenty other PFAAs) (rs6966061). MyGeneLog™. https://www.mygenelog.com/variants/rs6966061

← See all variants