Standard
Homeostasis model assessment of beta-cell function (dietary factor interaction)
LOC100132037 · rs2421332
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 Homeostasis model assessment of beta-cell function (dietary factor interaction) compared to the general population.
C/T
Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Homeostasis model assessment of beta-cell function (dietary factor interaction).
T/T
Published research associates this genotype with typical/baseline likelihood of Homeostasis model assessment of beta-cell function (dietary factor interaction) — no copies of the reported risk allele.
Source
Genome-wide contribution of genotype by environment interaction to variation of diabetes-related traits
Zheng JS,
Arnett DK,
Lee YC,
Shen J,
Parnell LD,
Smith CE,
Richardson K,
Li D,
Borecki IB,
Ordovás JM,
Lai CQ
PloS one · 2013 · PMID 24204828 · open access
Questions about rs2421332
What is rs2421332?
rs2421332 is a single position in the genome, in or near the LOC100132037 gene. Published research associates it with homeostasis model assessment of beta-cell function (dietary factor interaction). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs2421332 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 rs2421332 come from?
GWAS Catalog, PLoS One 2013, PMID:24204828. 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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