Standard
Glucosuria (mild)
SLC5A2 · rs141627694
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 (two copies of the reported risk allele) with a higher likelihood of Glucosuria (mild) compared to the general population.
C/T
Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Glucosuria (mild).
T/T
Published research associates this genotype with typical/baseline likelihood of Glucosuria (mild) — no copies of the reported risk allele.
Source
Sequence variants associating with urinary biomarkers
Benonisdottir S,
Kristjansson RP,
Oddsson A,
Steinthorsdottir V,
Mikaelsdottir E,
Kehr B,
Jensson BO,
Arnadottir GA,
Sulem G,
Sveinbjornsson G,
Kristmundsdottir S,
Ivarsdottir EV
and 26 more — show all
Tragante V,
Gunnarsson B,
Runolfsdottir HL,
Arthur JG,
Deaton AM,
Eyjolfsson GI,
Davidsson OB,
Asselbergs FW,
Hreidarsson AB,
Rafnar T,
Thorleifsson G,
Edvardsson V,
Sigurdsson G,
Helgadottir A,
Halldorsson BV,
Masson G,
Holm H,
Onundarson PT,
Indridason OS,
Benediktsson R,
Palsson R,
Gudbjartsson DF,
Olafsson I,
Thorsteinsdottir U,
Sulem P,
Stefansson K
Human molecular genetics · 2019 · PMID 30476138 · open access
Questions about rs141627694
What is rs141627694?
rs141627694 is a single position in the genome, in or near the SLC5A2 gene. Published research associates it with glucosuria (mild). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs141627694 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 rs141627694 come from?
GWAS Catalog, Hum Mol Genet 2019, PMID:30476138. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
← See all variants