Standard

Albumin in pregnancy

ALB · rs60904764

What the study found

Who was studied 97,444 Chinese ancestry individuals; replicated in 47,278 Chinese ancestry individuals.

The effect Each copy of the A allele shifted the measure 0.108 lower (95% confidence interval 0.078-0.138); p = 1 × 10−12.

How common The A allele had a frequency of about 9% in the people studied.

What each result means

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

Questions about rs60904764

What is rs60904764?

rs60904764 is a single position in the genome, in or near the ALB gene. Published research associates it with albumin in pregnancy. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs60904764 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 rs60904764 come from?

GWAS Catalog, Nature genetics 2026, PMID:42509370. 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 in pregnancy (rs60904764). MyGeneLog™. https://www.mygenelog.com/variants/rs60904764

← See all variants