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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 18,070 European ancestry individuals.
The effect
Each copy of the T allele shifted the measure 0.0875 lower (95% confidence interval 0.065-0.11); p = 8 × 10−15.
How common The T allele had a frequency of about 69% in the people studied.
Where it sits Chromosome 9, band 9p21.1 — in an intron of B4GALT1.
What ClinVar records
ClassificationBenign; criteria provided, single submitter (1 of 4 stars, 1 submitter), last evaluated 2018-09-05.
ClinVar record 1237475NM_001497.4(B4GALT1):c.413-212A>G
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/CNo copy of the version the research linked to Serum uromodulin levels (aptamer-based assay). This is the starting point the study compared everyone against.
C/TOne copy of the version the research linked to Serum uromodulin levels (aptamer-based assay). That is a smaller link than two copies.
T/TTwo copies of the version the research linked to Serum uromodulin levels (aptamer-based assay). That is the strongest link of the three results. A link in a study is not a diagnosis.
rs10738906 is a single position in the genome, in or near the B4GALT1 gene. Published research associates it with serum uromodulin levels (aptamer-based assay). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs10738906 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 rs10738906 come from?
GWAS Catalog, JCI insight 2022, PMID:35446786. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
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