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Systolic blood pressure

TARID · rs76987554

Where this position leads

Condition: Blood Pressure

rs76987554 Condition: Blood Pressure Blood Pressure Condition rs76987554 rs76987554 TARID

What each result means

C/C Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Systolic blood 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 Systolic blood pressure.
T/T Published research associates this genotype with typical/baseline likelihood of Systolic blood 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 rs76987554

What is rs76987554?

rs76987554 is a single position in the genome, in or near the TARID gene. Published research associates it with systolic blood pressure. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs76987554 linked to?

On MyGeneLog this position is linked to Blood Pressure. The research behind each link, and its sources, are set out on that condition page.

Does having rs76987554 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 rs76987554 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.

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