Standard
Hypertension
SLC12A9 · rs7801190
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 Hypertension compared to the general population. (GWAS Catalog, PLoS Genet 2011, PMID:21347282)
C/G
Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Hypertension. (GWAS Catalog, PLoS Genet 2011, PMID:21347282)
G/G
Published research associates this genotype with typical/baseline likelihood of Hypertension — no copies of the reported risk allele. (GWAS Catalog, PLoS Genet 2011, PMID:21347282)
Source
Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project
Lettre G,
Palmer CD,
Young T,
Ejebe KG,
Allayee H,
Benjamin EJ,
Bennett F,
Bowden DW,
Chakravarti A,
Dreisbach A,
Farlow DN,
Folsom AR
and 48 more — show all
Fornage M,
Forrester T,
Fox E,
Haiman CA,
Hartiala J,
Harris TB,
Hazen SL,
Heckbert SR,
Henderson BE,
Hirschhorn JN,
Keating BJ,
Kritchevsky SB,
Larkin E,
Li M,
Rudock ME,
McKenzie CA,
Meigs JB,
Meng YA,
Mosley TH,
Newman AB,
Newton-Cheh CH,
Paltoo DN,
Papanicolaou GJ,
Patterson N,
Post WS,
Psaty BM,
Qasim AN,
Qu L,
Rader DJ,
Redline S,
Reilly MP,
Reiner AP,
Rich SS,
Rotter JI,
Liu Y,
Shrader P,
Siscovick DS,
Tang WH,
Taylor HA,
Tracy RP,
Vasan RS,
Waters KM,
Wilks R,
Wilson JG,
Fabsitz RR,
Gabriel SB,
Kathiresan S,
Boerwinkle E
PLoS genetics · 2011 · PMID 21347282 · open access
Questions about rs7801190
What is rs7801190?
rs7801190 is a single position in the genome, in or near the SLC12A9 gene. Published research associates it with hypertension. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs7801190 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 rs7801190 come from?
GWAS Catalog, PLoS Genet 2011, PMID:21347282. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
← See all variants