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IDP T1 FAST ROIs V cerebellum VI

MACROD2 · rs2024900

What the study found

Who was studied 22,133 British ancestry individuals; replicated in 11,086 British ancestry individuals.

The effect Each copy of the T allele shifted the measure 0.068 higher (95% confidence interval 0.048-0.088); p = 1 × 10−12.

How common The T allele had a frequency of about 43% in the people studied.

Where it sits Chromosome 20, band 20p12.1 — in an intron of MACROD2.

What each result means

C/C Published research associates this genotype with typical/baseline likelihood of IDP T1 FAST ROIs V cerebellum VI — 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 IDP T1 FAST ROIs V cerebellum VI.
T/T Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of IDP T1 FAST ROIs V cerebellum VI compared to the general population.
Source

Questions about rs2024900

What is rs2024900?

rs2024900 is a single position in the genome, in or near the MACROD2 gene. Published research associates it with idp t1 fast rois v cerebellum vi. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs2024900 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 rs2024900 come from?

GWAS Catalog, Nature neuroscience 2021, PMID:33875891. 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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IDP T1 FAST ROIs V cerebellum VI (rs2024900). MyGeneLog™. https://www.mygenelog.com/variants/rs2024900

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