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Platelet crit (UKB data field 30090)

NAV3 · rs60232238

Where this position leads

Condition: Celiac Disease

rs60232238 Condition: Celiac Disease Celiac Disease Condition rs60232238 rs60232238 NAV3

What the study found

Who was studied 394,642 European ancestry individuals.

The effect Each copy of the C allele shifted the measure 0.0152 lower (95% confidence interval 0.011-0.02); p = 4 × 10−13.

How common The C allele had a frequency of about 23% in the people studied.

Where it sits Chromosome 12, band 12q21.2 — inside NAV3.

What each result means

C/C Two copies of the version the research linked to Platelet crit (UKB data field 30090). That is the strongest link of the three results. A link in a study is not a diagnosis.
C/G One copy of the version the research linked to Platelet crit (UKB data field 30090). That is a smaller link than two copies.
G/G No copy of the version the research linked to Platelet crit (UKB data field 30090). This is the starting point the study compared everyone against.
Source

Questions about rs60232238

What is rs60232238?

rs60232238 is a single position in the genome, in or near the NAV3 gene. Published research associates it with platelet crit (ukb data field 30090). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs60232238 linked to?

On MyGeneLog this position is linked to Celiac Disease. The research behind each link, and its sources, are set out on that condition page.

Does having rs60232238 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 rs60232238 come from?

GWAS Catalog, Nature genetics 2025, PMID:39789286. 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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Platelet crit (UKB data field 30090) (rs60232238). MyGeneLog™. https://www.mygenelog.com/variants/rs60232238

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