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Cerebrospinal fluid p-tau levels in normal amyloid levels

near GMNC · rs10937450

What the study found

Who was studied 3,174 European ancestry individuals.

The effect Each copy of the C allele shifted the measure 6.71 z score higher; p = 2 × 10−11.

How common The C allele had a frequency of about 39% in the people studied.

Where it sits Chromosome 3, band 3q28 — between genes, 42.1 kb from GMNC.

What each result means

C/C Two copies of the version the research linked to Cerebrospinal fluid p-tau levels in normal amyloid levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
C/G One copy of the version the research linked to Cerebrospinal fluid p-tau levels in normal amyloid levels. That is a smaller link than two copies.
G/G No copy of the version the research linked to Cerebrospinal fluid p-tau levels in normal amyloid levels. This is the starting point the study compared everyone against.
Source

Questions about rs10937450

What is rs10937450?

rs10937450 is a single position in the genome, in or near the near GMNC gene. Published research associates it with cerebrospinal fluid p-tau levels in normal amyloid levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs10937450 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 rs10937450 come from?

GWAS Catalog, Acta neuropathologica 2022, PMID:36066633. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

Quoting this page

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Cerebrospinal fluid p-tau levels in normal amyloid levels (rs10937450). MyGeneLog™. https://www.mygenelog.com/variants/rs10937450

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