CUBN · rs144360241
Where this position leads
Condition: Kidney Function
What the study found
Who was studied 382,500 European ancestry individuals.
The effect Each copy of the C allele shifted the measure 0.0819 higher (95% confidence interval 0.058-0.106); p = 3 × 10−11.
How common The C allele had a frequency of about 0% in the people studied.
Where it sits Chromosome 10, band 10p13 — a missense change in CUBN.
What ClinVar records
Classification
Benign/Likely benign for Imerslund-Grasbeck syndrome, Imerslund-Grasbeck syndrome type 1; criteria provided, multiple submitters, no conflicts (2 of 4 stars, 8 submitters), last evaluated 2026-01-14.
ClinVar record 695565 NM_001081.4(CUBN):c.6469A>G (p.Asn2157Asp)
What this is ClinVar's aggregate record for this position (as of its 2026-10-19 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 people read about alongside this
Papers in Europe PMC whose title or abstract names both this rsID and that subject. A shared paper means somebody wrote about the two together — it is not a claim that this position explains the subject.
rs144360241 is a single position in the genome, in or near the CUBN gene. Published research associates it with urinary albumin excretion. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
On MyGeneLog this position is linked to Kidney Function. The research behind each link, and its sources, are set out on that condition page.
Subjects that appear in the title or abstract of the same papers as this rsID include blood sugar and insulin (1 papers), kidneys (1 papers). A shared paper means somebody wrote about the two together; it is not a claim that this position explains the topic.
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.
GWAS Catalog, Am J Hum Genet 2018, PMID:30220432. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
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.
Urinary albumin excretion (rs144360241). MyGeneLog™. https://www.mygenelog.com/variants/rs144360241