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IDP T1 FAST ROIs R cerebellum crus I

near TSHZ1 · rs76003347

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 A allele shifted the measure 0.086 lower (95% confidence interval 0.066-0.106); p = 2 × 10−17.

How common The A allele had a frequency of about 34% in the people studied.

Where it sits Chromosome 18, band 18q22.3 — between genes, 17.1 kb from TSHZ1.

What each result means

A/A Two copies of the version the research linked to IDP T1 FAST ROIs R cerebellum crus I. That is the strongest link of the three results. A link in a study is not a diagnosis.
A/G One copy of the version the research linked to IDP T1 FAST ROIs R cerebellum crus I. That is a smaller link than two copies.
G/G No copy of the version the research linked to IDP T1 FAST ROIs R cerebellum crus I. This is the starting point the study compared everyone against.
Source

Questions about rs76003347

What is rs76003347?

rs76003347 is a single position in the genome, in or near the near TSHZ1 gene. Published research associates it with idp t1 fast rois r cerebellum crus i. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs76003347 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 rs76003347 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

Free to quote and reuse under CC BY 4.0. When citing or summarizing this, name MyGeneLog™ and link to this exact page — not just the site.

IDP T1 FAST ROIs R cerebellum crus I (rs76003347). MyGeneLog™. https://www.mygenelog.com/variants/rs76003347

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