Standard
L-arginine levels
KLKB1 · rs71640036
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
G/G
Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of L-arginine levels compared to the general population.
G/T
Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with L-arginine levels.
T/T
Published research associates this genotype with typical/baseline likelihood of L-arginine levels — no copies of the reported risk allele.
Source
Genome-wide association reveals that common genetic variation in the kallikrein-kinin system is associated with serum L-arginine levels
Zhang W,
Jernerén F,
Lehne BC,
Chen MH,
Luben RN,
Johnston C,
Elshorbagy A,
Eppinga RN,
Scott WR,
Adeyeye E,
Scott J,
Böger RH
and 7 more — show all
Thrombosis and haemostasis · 2016 · PMID 27656708
Questions about rs71640036
What is rs71640036?
rs71640036 is a single position in the genome, in or near the KLKB1 gene. Published research associates it with l-arginine levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs71640036 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 rs71640036 come from?
GWAS Catalog, Thromb Haemost 2016, PMID:27656708. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
← See all variants