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HDL cholesterol x physical activity interaction (2df test)

DDB2 · rs326222

Where this position leads

Condition: Cholesterol (LDL, HDL and Total)

rs326222 Condition: Cholesterol (LDL, HDL and Total) Cholesterol (LDL, HDL and Total) Condition rs326222 rs326222 DDB2

What the study found

Who was studied 7,395 African American inactive individuals, 13,092 African American active individuals, 2,753 Asian ancestry inactive individuals, 3,650 Asian ancestry active individuals, 22,963 European ancestry inactive individuals, 61,939 European ancestry active individuals, 2,829 Hispanic or Latin American inactive individuals, 6,358 Hispanic or Latin American active individuals; replicated in 1,886 African American inactive individuals, 1,892 African American active individuals, 1,217 South African Black ancestry inactive individuals, 389 South African Black ancestry active individuals, 2,494 East Asian ancestry inactive individuals, 1,947 East Asian ancestry active individuals, 724 South Asian ancestry inactive individuals, 1,425 South Asian ancestry active individuals, 41,042 European ancestry inactive individuals, 66,575 European ancestry active individuals, 2,619 Hispanic inactive individuals, 8,802 Hispanic active individuals.

The effect The reported allele is T; the catalogue records no effect size ; p = 7 × 10−29.

How common The T allele had a frequency of about 36% in the people studied.

Where it sits Chromosome 11, band 11p11.2 — in an intron of DDB2.

What ClinVar records

Classification Benign for Xeroderma pigmentosum, group E; criteria provided, multiple submitters, no conflicts (2 of 4 stars, 3 submitters), last evaluated 2021-07-30. ClinVar record 1237094 NM_000107.3(DDB2):c.1189-21T>C

What this is ClinVar's aggregate record for this position (as of its 2026-10-12 release), not a result about you. A classification describes the variant against the condition named, as laboratories submitted it. Whether a person carries this variant, and what that would mean for them, is a question for a clinical test and a genetic counsellor.

What each result means

C/C No copy of the version the research linked to HDL cholesterol x physical activity interaction (2df test). This is the starting point the study compared everyone against.
C/T One copy of the version the research linked to HDL cholesterol x physical activity interaction (2df test). That is a smaller link than two copies.
T/T Two copies of the version the research linked to HDL cholesterol x physical activity interaction (2df test). That is the strongest link of the three results. A link in a study is not a diagnosis.
Source

Questions about rs326222

What is rs326222?

rs326222 is a single position in the genome, in or near the DDB2 gene. Published research associates it with hdl cholesterol x physical activity interaction (2df test). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs326222 linked to?

On MyGeneLog this position is linked to Cholesterol (LDL, HDL and Total). The research behind each link, and its sources, are set out on that condition page.

Does having rs326222 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 rs326222 come from?

GWAS Catalog, Nat Commun 2019, PMID:30670697. 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.

HDL cholesterol x physical activity interaction (2df test) (rs326222). MyGeneLog™. https://www.mygenelog.com/variants/rs326222

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