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Serum levels of protein GRAMD1C

GRAMD1C · rs61634901

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 5,366 Icelandic ancestry individuals.

The effect Each copy of the A allele shifted the measure 0.639 higher (95% confidence interval 0.6-0.68); p = 1 × 10⁻²⁶².

How common The A allele had a frequency of about 34% in the people studied.

Where it sits Chromosome 3, band 3q13.31 — in an intron of GRAMD1C.

What each result means

A/A Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Serum levels of protein GRAMD1C compared to the general population.

A/G Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Serum levels of protein GRAMD1C.

G/G Published research associates this genotype with typical/baseline likelihood of Serum levels of protein GRAMD1C — no copies of the reported risk allele.

Source

A genome-wide association study of serum proteins reveals shared loci with common diseases

Gudjonsson A, Gudmundsdottir V, Axelsson GT, Gudmundsson EF, Jonsson BG, Launer LJ, Lamb JR, Jennings LL, Aspelund T, Emilsson V, Gudnason V

Nature communications · 2022 · PMID 35078996 · open access

Questions about rs61634901

What is rs61634901?

rs61634901 is a single position in the genome, in or near the GRAMD1C gene. Published research associates it with serum levels of protein gramd1c. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs61634901 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 rs61634901 come from?

GWAS Catalog, Nature communications 2022, PMID:35078996. 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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Serum levels of protein GRAMD1C (rs61634901). MyGeneLog™. https://www.mygenelog.com/variants/rs61634901

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