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Rho GTPase-activating protein 30 levels

LINC01322 · rs62295996

What the study found

Who was studied 10,708 European ancestry individuals.

The effect Each copy of the A allele shifted the measure 0.303 lower (95% confidence interval 0.27-0.33); p = 2 × 10−86.

How common The A allele had a frequency of about 21% in the people studied.

Where it sits Chromosome 3, band 3q26.1 — in an intron of LINC01322.

What each result means

A/A Two copies of the version the research linked to Rho GTPase-activating protein 30 levels. 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 Rho GTPase-activating protein 30 levels. That is a smaller link than two copies.
G/G No copy of the version the research linked to Rho GTPase-activating protein 30 levels. This is the starting point the study compared everyone against.
Source

Questions about rs62295996

What is rs62295996?

rs62295996 is a single position in the genome, in or near the LINC01322 gene. Published research associates it with rho gtpase-activating protein 30 levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs62295996 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 rs62295996 come from?

GWAS Catalog, Science (New York, N.Y.) 2021, PMID:34648354. 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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Rho GTPase-activating protein 30 levels (rs62295996). MyGeneLog™. https://www.mygenelog.com/variants/rs62295996

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