Standard
Glomerular filtration rate
SLC34A1 · rs35716097
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 Glomerular filtration rate — 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 Glomerular filtration rate.
T/T
Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Glomerular filtration rate compared to the general population.
Source
Trans-ethnic Fine Mapping Highlights Kidney-Function Genes Linked to Salt Sensitivity
Mahajan A,
Rodan AR,
Le TH,
Gaulton KJ,
Haessler J,
Stilp AM,
Kamatani Y,
Zhu G,
Sofer T,
Puri S,
Schellinger JN,
Chu PL
and 26 more — show all
Cechova S,
van Zuydam N,
Arnlov J,
Flessner MF,
Giedraitis V,
Heath AC,
Kubo M,
Larsson A,
Lindgren CM,
Madden PAF,
Montgomery GW,
Papanicolaou GJ,
Reiner AP,
Sundström J,
Thornton TA,
Lind L,
Ingelsson E,
Cai J,
Martin NG,
Kooperberg C,
Matsuda K,
Whitfield JB,
Okada Y,
Laurie CC,
Morris AP,
Franceschini N
American journal of human genetics · 2016 · PMID 27588450 · open access
Questions about rs35716097
What is rs35716097?
rs35716097 is a single position in the genome, in or near the SLC34A1 gene. Published research associates it with glomerular filtration rate. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs35716097 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 rs35716097 come from?
GWAS Catalog, Am J Hum Genet 2016, PMID:27588450. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
← See all variants