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T1 CAT volume L IX

RELN · rs631929

What the study found

Who was studied 7,058 Chinese Han ancestry individuals.

The effect Each copy of the G allele shifted the measure 0.108 higher (95% confidence interval 0.073-0.143); p = 1 × 10−9.

Where it sits Chromosome 7, band 7q22.1 — in an intron of RELN.

What each result means

A/A No copy of the version the research linked to T1 CAT volume L IX. This is the starting point the study compared everyone against.
A/G One copy of the version the research linked to T1 CAT volume L IX. That is a smaller link than two copies.
G/G Two copies of the version the research linked to T1 CAT volume L IX. That is the strongest link of the three results. A link in a study is not a diagnosis.
Source

Questions about rs631929

What is rs631929?

rs631929 is a single position in the genome, in or near the RELN gene. Published research associates it with t1 cat volume l ix. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs631929 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 rs631929 come from?

GWAS Catalog, Nature genetics 2024, PMID:38811844. 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.

T1 CAT volume L IX (rs631929). MyGeneLog™. https://www.mygenelog.com/variants/rs631929

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