Sensitive

Systemic lupus erythematosus

C2 · rs558702

Where this position leads

Condition: Systemic Lupus Erythematosus

rs558702 Condition: Systemic Lupus Erythematosus Systemic Lupus Erythematosus Condition rs558702 rs558702 C2

Strength of the evidence

2 / 4

Its strongest genetic-study result is p = 10−21, 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 725 European ancestry cases, 2,438 European ancestry controls.

The effect Each copy of the A allele carried 2.28 times the odds of Systemic lupus erythematosus (95% confidence interval 2.097-2.47); p = 8 × 10−21.

How common The A allele had a frequency of about 10% in the people studied.

Where it sits Chromosome 6, band 6p21.33 — in an intron of C2.

How common each version is

AG
World gnomAD
A 7.5% · G 92.5%
World 1000 Genomes
A 3.4% · G 96.7%
World TOPMed
A 7.1% · G 92.9%

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. No Korean figure for this position yet.

What each result means

A/A Two copies of the version the research linked to Systemic lupus erythematosus. 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 Systemic lupus erythematosus. That is a smaller link than two copies.
G/G No copy of the version the research linked to Systemic lupus erythematosus. This is the starting point the study compared everyone against.
Source

Questions about rs558702

What is rs558702?

rs558702 is a single position in the genome, in or near the C2 gene. Published research associates it with systemic lupus erythematosus. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs558702 linked to?

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

Does having rs558702 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 rs558702 come from?

GWAS Catalog, Genes Immun 2014, PMID:24871463. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

Quoting this page

Licensed CC BY-NC 4.0: free to read, share and adapt for non-commercial use, naming MyGeneLog™ and linking the exact page. Commercial use, including training or serving a commercial AI system, needs a licence — https://www.mygenelog.com/license

Systemic lupus erythematosus (rs558702). MyGeneLog™. https://www.mygenelog.com/variants/rs558702

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