Standard
Serum magnesium levels
MUC1 · rs4460629
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 each result means
C/C
Published research associates this genotype with typical/baseline likelihood of Serum magnesium levels — no copies of the reported risk allele.
C/T
Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Serum magnesium levels.
T/T
Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Serum magnesium levels compared to the general population.
Source
Genome-Wide Meta-Analysis Unravels Interactions between Magnesium Homeostasis and Metabolic Phenotypes
Corre T,
Arjona FJ,
Hayward C,
Youhanna S,
de Baaij JHF,
Belge H,
Nägele N,
Debaix H,
Blanchard MG,
Traglia M,
Harris SE,
Ulivi S
and 29 more — show all
Rueedi R,
Lamparter D,
Macé A,
Sala C,
Lenarduzzi S,
Ponte B,
Pruijm M,
Ackermann D,
Ehret G,
Baptista D,
Polasek O,
Rudan I,
Hurd TW,
Hastie ND,
Vitart V,
Waeber G,
Kutalik Z,
Bergmann S,
Vargas-Poussou R,
Konrad M,
Gasparini P,
Deary IJ,
Starr JM,
Toniolo D,
Vollenweider P,
Hoenderop JGJ,
Bindels RJM,
Bochud M,
Devuyst O
Journal of the American Society of Nephrology : JASN · 2018 · PMID 29093028
Questions about rs4460629
What is rs4460629?
rs4460629 is a single position in the genome, in or near the MUC1 gene. Published research associates it with serum magnesium levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs4460629 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 rs4460629 come from?
GWAS Catalog, J Am Soc Nephrol 2017, PMID:29093028. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
← See all variants