KMT2A · rs9332801
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 2,083,151 European ancestry individuals; replicated in 287,239 European ancestry individuals.
The effect Each copy of the C allele shifted the measure 0.0109 higher (95% confidence interval 0.0072-0.0146); p = 6 × 10−9.
How common The C allele had a frequency of about 6% in the people studied.
Where it sits Chromosome 11, band 11q23.3 — a synonymous change in KMT2A.
What ClinVar records
Classification
Benign; criteria provided, multiple submitters, no conflicts (2 of 4 stars, 7 submitters), last evaluated 2026-02-04.
ClinVar record 158702 NM_001197104.2(KMT2A):c.4284A>C (p.Ile1428=)
What this is ClinVar's aggregate record for this position (as of its 2026-09-24 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.
rs9332801 is a single position in the genome, in or near the KMT2A gene. Published research associates it with well-being spectrum (multivariate analysis). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
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, Nat Genet 2019, PMID:30643256. 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.
Well-being spectrum (multivariate analysis) (rs9332801). MyGeneLog™. https://www.mygenelog.com/variants/rs9332801