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Annualised percent change of cerebrospinal fluid AB1-42 levels

CBFA2T3 · rs13333659

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 with typical/baseline likelihood of Annualised percent change of cerebrospinal fluid AB1-42 levels — no copies of the reported risk allele.

G/T Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Annualised percent change of cerebrospinal fluid AB1-42 levels.

T/T Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Annualised percent change of cerebrospinal fluid AB1-42 levels compared to the general population.

Source

Genome-wide association study identifies <i>CBFA2T3</i> affecting the rate of CSF Aβ<sub>42</sub> decline in non-demented elders

Dou KX, Zhang C, Tan CC, Xu W, Li JQ, Cao XP, Tan L, Yu JT

Alzheimer’s Disease Neuroimaging Initiative (ADNI)

Aging · 2019 · PMID 31370031 · open access

Questions about rs13333659

What is rs13333659?

rs13333659 is a single position in the genome, in or near the CBFA2T3 gene. Published research associates it with annualised percent change of cerebrospinal fluid ab1-42 levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs13333659 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 rs13333659 come from?

GWAS Catalog, Aging (Albany NY) 2019, PMID:31370031. 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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