Standard

Low density lipoprotein cholesterol levels

POC5 · rs34361

Where this position leads

Condition: Cholesterol (LDL, HDL and Total)

rs34361 Condition: Cholesterol (LDL, HDL and Total) Cholesterol (LDL, HDL and Total) Condition rs34361 rs34361 POC5

Strength of the evidence

2 / 4

Its strongest genetic-study result is p = 10−35, with 4 associations in the GWAS Catalog.

How this is scored

4: ClinVar disease-causing, reviewed by an expert panel or a guideline (3–4 stars). 3: ClinVar, several labs agreeing (2 stars), or a genetic study at p ≤ 10−50. 2: ClinVar from one lab (1 star), or p ≤ 10−20. 1: ClinVar submitted without criteria (0 stars), or genome-wide significance (p ≤ 5×10−8). The higher of the two counts. It says how solid the evidence is, not whether it matters for a particular person.

What the study found

Who was studied 76,627 European ancestry individuals, 7,795 Hispanic individuals, 6,855 East Asian ancestry individuals, 2,958 African American individuals, 439 South Asian ancestry individuals.

The effect Each copy of the A allele shifted the measure 0.055 higher; p = 9 × 10−36.

Where it sits Chromosome 5, band 5q13.3 — in an intron of POC5.

How common each version is

AG
Korean KRGDB
A 67.1% · G 32.9%
Korean Korea4K
A 66.9% · G 33.1%
Korean Korea1K
A 65.7% · G 34.3%
Japanese ToMMo
A 68.8% · G 31.2%
Vietnamese
A 64.3% · G 35.6%
World gnomAD
A 42.1% · G 57.9%
World 1000 Genomes
A 51.0% · G 49.0%
World TOPMed
A 41.6% · G 58.4%

The share of all copies of this position that are each version. Source: the population studies published in dbSNP (US NCBI); each row names its study.

What each result means

A/A Two copies of the version the research linked to Low density lipoprotein cholesterol 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 Low density lipoprotein cholesterol levels. That is a smaller link than two copies.
G/G No copy of the version the research linked to Low density lipoprotein cholesterol levels. This is the starting point the study compared everyone against.
Source

Questions about rs34361

What is rs34361?

rs34361 is a single position in the genome, in or near the POC5 gene. Published research associates it with low density lipoprotein cholesterol levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs34361 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 rs34361 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 rs34361 come from?

GWAS Catalog, Nat Genet 2018, PMID:29507422. 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.

Low density lipoprotein cholesterol levels (rs34361). MyGeneLog™. https://www.mygenelog.com/variants/rs34361

← See all variants