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Phosphoglucomutase-1 levels

PGM1 · rs1126728

What the study found

Who was studied 3,506 European ancestry individuals.

The effect Each copy of the T allele shifted the measure 0.167 higher (95% confidence interval 0.12-0.22); p = 2 × 10−10.

How common The T allele had a frequency of about 24% in the people studied.

Where it sits Chromosome 1, band 1p31.3 — a missense change in PGM1.

What ClinVar records

Classification Benign/Likely benign for PGM1-congenital disorder of glycosylation; criteria provided, multiple submitters, no conflicts (2 of 4 stars, 10 submitters), last evaluated 2026-02-04. ClinVar record 297874 NM_002633.3(PGM1):c.661C>T (p.Arg221Cys)

What this is ClinVar's aggregate record for this position (as of its 2026-10-12 release), not a result about you. A classification describes the variant against the condition named, as laboratories submitted it. Whether a person carries this variant, and what that would mean for them, is a question for a clinical test and a genetic counsellor.

What each result means

C/C No copy of the version the research linked to Phosphoglucomutase-1 levels. This is the starting point the study compared everyone against.
C/T One copy of the version the research linked to Phosphoglucomutase-1 levels. That is a smaller link than two copies.
T/T Two copies of the version the research linked to Phosphoglucomutase-1 levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
Source

Questions about rs1126728

What is rs1126728?

rs1126728 is a single position in the genome, in or near the PGM1 gene. Published research associates it with phosphoglucomutase-1 levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs1126728 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 rs1126728 come from?

GWAS Catalog, Nature genetics 2024, PMID:39528825. 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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Phosphoglucomutase-1 levels (rs1126728). MyGeneLog™. https://www.mygenelog.com/variants/rs1126728

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