Standard
Pulse pressure
LLPH · rs113866309
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 Pulse pressure compared to the general population.
C/T
Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Pulse pressure.
T/T
Published research associates this genotype with typical/baseline likelihood of Pulse pressure — no copies of the reported risk allele.
Source
Single-trait and multi-trait genome-wide association analyses identify novel loci for blood pressure in African-ancestry populations
Liang J,
Le TH,
Edwards DRV,
Tayo BO,
Gaulton KJ,
Smith JA,
Lu Y,
Jensen RA,
Chen G,
Yanek LR,
Schwander K,
Tajuddin SM
and 69 more — show all
Sofer T,
Kim W,
Kayima J,
McKenzie CA,
Fox E,
Nalls MA,
Young JH,
Sun YV,
Lane JM,
Cechova S,
Zhou J,
Tang H,
Fornage M,
Musani SK,
Wang H,
Lee J,
Adeyemo A,
Dreisbach AW,
Forrester T,
Chu PL,
Cappola A,
Evans MK,
Morrison AC,
Martin LW,
Wiggins KL,
Hui Q,
Zhao W,
Jackson RD,
Ware EB,
Faul JD,
Reiner AP,
Bray M,
Denny JC,
Mosley TH,
Palmas W,
Guo X,
Papanicolaou GJ,
Penman AD,
Polak JF,
Rice K,
Rice K,
Taylor KD,
Boerwinkle E,
Bottinger EP,
Liu K,
Risch N,
Hunt SC,
Kooperberg C,
Zonderman AB,
Laurie CC,
Becker DM,
Cai J,
Loos RJF,
Psaty BM,
Weir DR,
Kardia SLR,
Arnett DK,
Won S,
Edwards TL,
Redline S,
Cooper RS,
Rao DC,
Rotter JI,
Rotimi C,
Levy D,
Chakravarti A,
Zhu X,
Franceschini N,
Franceschini N
PLoS genetics · 2017 · PMID 28498854 · open access
Questions about rs113866309
What is rs113866309?
rs113866309 is a single position in the genome, in or near the LLPH gene. Published research associates it with pulse pressure. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs113866309 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 rs113866309 come from?
GWAS Catalog, PLoS Genet 2017, PMID:28498854. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
← See all variants