Sensitive

Systemic lupus erythematosus

GATA4 · rs745379

Where this position leads

Condition: Systemic Lupus Erythematosus

rs745379 Condition: Systemic Lupus Erythematosus Systemic Lupus Erythematosus Condition rs745379 rs745379 GATA4

What the study found

Who was studied 16,491 European ancestry cases, 1,202,106 European ancestry controls, 5,051 East Asian ancestry cases, 185,362 East Asian ancestry controls, 740 African American or Afro-Caribbean cases, 120,993 African American or Afro-Caribbean controls, 212 Hispanic or Latin American cases, 59,641 Hispanic or Latin American controls.

The effect Each copy of the G allele shifted the measure 0.0989 lower (95% confidence interval 0.065-0.133); p = 7 × 10−12.

Where it sits Chromosome 8, band 8p23.1 — in an intron of GATA4.

What ClinVar records

Classification Benign for Congenital heart disease; criteria provided, multiple submitters, no conflicts (2 of 4 stars, 8 submitters), last evaluated 2025-02-16. ClinVar record 433015 NM_001308093.3(GATA4):c.1150-107A>G

What this is ClinVar's aggregate record for this position (as of its 2026-10-19 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

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

Questions about rs745379

What is rs745379?

rs745379 is a single position in the genome, in or near the GATA4 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 rs745379 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 rs745379 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 rs745379 come from?

GWAS Catalog, Mammalian genome : official journal of the International Mammalian Genome Society 2026, PMID:42581184. 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.

Systemic lupus erythematosus (rs745379). MyGeneLog™. https://www.mygenelog.com/variants/rs745379

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