Standard
Plasma homocysteine levels (post-methionine load test)
GNMT · rs9296404
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 homocysteine levels (post-methionine load test) — 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 homocysteine levels (post-methionine load test).
T/T
Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Plasma homocysteine levels (post-methionine load test) compared to the general population.
Source
Genome-wide meta-analysis of homocysteine and methionine metabolism identifies five one carbon metabolism loci and a novel association of ALDH1L1 with ischemic stroke
Williams SR,
Yang Q,
Chen F,
Liu X,
Keene KL,
Jacques P,
Chen WM,
Weinstein G,
Hsu FC,
Beiser A,
Wang L,
Bookman E
and 9 more — show all
PLoS genetics · 2014 · PMID 24651765 · open access
Questions about rs9296404
What is rs9296404?
rs9296404 is a single position in the genome, in or near the GNMT gene. Published research associates it with plasma homocysteine levels (post-methionine load test). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs9296404 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 rs9296404 come from?
GWAS Catalog, PLoS Genet 2014, PMID:24651765. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
← See all variants