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IDP dMRI TBSS ICVF Retrolenticular part of internal capsule L

near HLA-DQB1 · rs57315130

What the study found

Who was studied 20,859 British ancestry individuals; replicated in 10,496 British ancestry individuals.

The effect Each copy of the A allele shifted the measure 0.085 higher (95% confidence interval 0.06-0.11); p = 2 × 10−11.

How common The A allele had a frequency of about 28% in the people studied.

Where it sits Chromosome 6, band 6p21.32 — between genes, 1.9 kb from HLA-DQB1.

What each result means

A/A Two copies of the version the research linked to IDP dMRI TBSS ICVF Retrolenticular part of internal capsule L. 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 dMRI TBSS ICVF Retrolenticular part of internal capsule L. That is a smaller link than two copies.
G/G No copy of the version the research linked to IDP dMRI TBSS ICVF Retrolenticular part of internal capsule L. This is the starting point the study compared everyone against.
Source

Questions about rs57315130

What is rs57315130?

rs57315130 is a single position in the genome, in or near the near HLA-DQB1 gene. Published research associates it with idp dmri tbss icvf retrolenticular part of internal capsule l. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs57315130 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 rs57315130 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 dMRI TBSS ICVF Retrolenticular part of internal capsule L (rs57315130). MyGeneLog™. https://www.mygenelog.com/variants/rs57315130

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