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Albumin levels (UKB data field 23479)

HSPA7 · rs200837054

What the study found

Who was studied 88,315 European ancestry individuals.

The effect Each copy of the T allele shifted the measure 0.0374 lower (95% confidence interval 0.027-0.048); p = 6 × 10−12.

How common The T allele had a frequency of about 29% in the people studied.

Where it sits Chromosome 1, band 1q23.3 — in a non-coding transcript of HSPA7.

What each result means

G/G No copy of the version the research linked to Albumin levels (UKB data field 23479). This is the starting point the study compared everyone against.
G/T One copy of the version the research linked to Albumin levels (UKB data field 23479). That is a smaller link than two copies.
T/T Two copies of the version the research linked to Albumin levels (UKB data field 23479). That is the strongest link of the three results. A link in a study is not a diagnosis.
Source

Questions about rs200837054

What is rs200837054?

rs200837054 is a single position in the genome, in or near the HSPA7 gene. Published research associates it with albumin levels (ukb data field 23479). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs200837054 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 rs200837054 come from?

GWAS Catalog, Biological psychiatry 2023, PMID:36764567. 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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Albumin levels (UKB data field 23479) (rs200837054). MyGeneLog™. https://www.mygenelog.com/variants/rs200837054

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