Standard
Plasma plasminogen levels
PLG · rs4252129
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 Plasma plasminogen levels — 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 Plasma plasminogen levels.
T/T
Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Plasma plasminogen levels compared to the general population.
Source
Genetic variants in PLG, LPA, and SIGLEC 14 as well as smoking contribute to plasma plasminogen levels
Ma Q,
Ozel AB,
Ramdas S,
McGee B,
Khoriaty R,
Siemieniak D,
Li HD,
Guan Y,
Brody LC,
Mills JL,
Molloy AM,
Ginsburg D
and 2 more — show all
Blood · 2014 · PMID 25208887
Questions about rs4252129
What is rs4252129?
rs4252129 is a single position in the genome, in or near the PLG gene. Published research associates it with plasma plasminogen levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs4252129 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 rs4252129 come from?
GWAS Catalog, Blood 2014, PMID:25208887. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
← See all variants