Standard

Albumin levels

near FCHO2 · rs628401

What the study found

Who was studied 104,632 British ancestry post-menopausal women.

The effect Each copy of the A allele shifted the measure 0.1 g/L lower (95% confidence interval 0.071-0.129); p = 1 × 10−11.

How common The A allele had a frequency of about 52% in the people studied.

Where it sits Chromosome 5, band 5q13.2 — between genes, 8.8 kb from FCHO2.

What each result means

A/A Two copies of the version the research linked to Albumin levels. 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 Albumin levels. That is a smaller link than two copies.
G/G No copy of the version the research linked to Albumin levels. This is the starting point the study compared everyone against.
Source

Questions about rs628401

What is rs628401?

rs628401 is a single position in the genome, in or near the near FCHO2 gene. Published research associates it with albumin levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs628401 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 rs628401 come from?

GWAS Catalog, Science advances 2021, PMID:34321204. 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.

Albumin levels (rs628401). MyGeneLog™. https://www.mygenelog.com/variants/rs628401

← See all variants