Sensitive

Developmental dysplasia of the hip or hip osteoarthritis

ERC2 · rs1519038

Where this position leads

Condition: Hip Osteoarthritis

rs1519038 Condition: Hip Osteoarthritis Hip Osteoarthritis Condition rs1519038 rs1519038 ERC2

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 T allele carried 0.94 times the odds of Developmental dysplasia of the hip or hip osteoarthritis (95% confidence interval 0.919-0.96); p = 3 × 10−8.

How common The T allele had a frequency of about 70% in the people studied.

Where it sits Chromosome 3, band 3p14.3 — in an intron of ERC2.

What each result means

C/C 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.
C/T 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.
T/T 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.
Source

Questions about rs1519038

What is rs1519038?

rs1519038 is a single position in the genome, in or near the ERC2 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 rs1519038 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 rs1519038 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 rs1519038 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 (rs1519038). MyGeneLog™. https://www.mygenelog.com/variants/rs1519038

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