Sensitive

Developmental dysplasia of the hip or hip osteoarthritis

LRIG3 · rs79056043

Where this position leads

Condition: Hip Osteoarthritis

rs79056043 Condition: Hip Osteoarthritis Hip Osteoarthritis Condition rs79056043 rs79056043 LRIG3

What the study found

Who was studied 36,445 European ancestry cases, 316,943 European ancestry controls, 1,085 Japanese ancestry cases, 24,000 Japanese ancestry controls.

The effect Each copy of the A allele carried 0.89 times the odds of Developmental dysplasia of the hip or hip osteoarthritis (95% confidence interval 0.863-0.927); p = 1 × 10−9.

How common The A allele had a frequency of about 94% in the people studied.

Where it sits Chromosome 12, band 12q14.1 — in an intron of LRIG3.

What each result means

A/A Two copies of the version the research linked to Developmental dysplasia of the hip or hip osteoarthritis. 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 Developmental dysplasia of the hip or hip osteoarthritis. That is a smaller link than two copies.
G/G No copy of the version the research linked to Developmental dysplasia of the hip or hip osteoarthritis. This is the starting point the study compared everyone against.
Source

Questions about rs79056043

What is rs79056043?

rs79056043 is a single position in the genome, in or near the LRIG3 gene. Published research associates it with developmental dysplasia of the hip or hip osteoarthritis. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs79056043 linked to?

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

Does having rs79056043 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 rs79056043 come from?

GWAS Catalog, Bone research 2026, PMID:41912496. 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.

Developmental dysplasia of the hip or hip osteoarthritis (rs79056043). MyGeneLog™. https://www.mygenelog.com/variants/rs79056043

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