Standard
Rate of cognitive decline in mild cognitive impairment (time interaction)
UBR5 · rs7840202
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
A/A
Published research associates this genotype with typical/baseline likelihood of Rate of cognitive decline in mild cognitive impairment (time interaction) — no copies of the reported risk allele.
A/C
Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Rate of cognitive decline in mild cognitive impairment (time interaction).
C/C
Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Rate of cognitive decline in mild cognitive impairment (time interaction) compared to the general population.
Source
Genome-wide association study identifies multiple novel loci associated with disease progression in subjects with mild cognitive impairment
Hu X,
Pickering EH,
Hall SK,
Naik S,
Liu YC,
Soares H,
Katz E,
Paciga SA,
Liu W,
Aisen PS,
Bales KR,
Samad TA
and 1 more — show all
Translational psychiatry · 2011 · PMID 22833209 · open access
Questions about rs7840202
What is rs7840202?
rs7840202 is a single position in the genome, in or near the UBR5 gene. Published research associates it with rate of cognitive decline in mild cognitive impairment (time interaction). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs7840202 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 rs7840202 come from?
GWAS Catalog, Transl Psychiatry 2011, PMID:22833209. 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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