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C-reactive protein levels

DNAJC6 · rs61753391

Where this position leads

Condition: C-Reactive Protein Levels

rs61753391 Condition: C-Reactive Protein Levels C-Reactive Protein Levels Condition rs61753391 rs61753391 DNAJC6

What the study found

Who was studied 341,805 European ancestry individuals, 6,006 African ancestry individuals, 7,316 South Asian ancestry individuals.

The effect Each copy of the A allele shifted the measure 0.0515 higher (95% confidence interval 0.037-0.066); p = 9 × 10−12.

Where it sits Chromosome 1, band 1p31.3 — a synonymous change in DNAJC6.

What ClinVar records

Classification Benign/Likely benign for Juvenile onset Parkinson disease 19A; criteria provided, multiple submitters, no conflicts (2 of 4 stars, 7 submitters), last evaluated 2026-02-02. ClinVar record 474681 NM_001256864.2(DNAJC6):c.678G>A (p.Ala226=)

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 Two copies of the version the research linked to C-reactive protein 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 C-reactive protein levels. That is a smaller link than two copies.
G/G No copy of the version the research linked to C-reactive protein levels. This is the starting point the study compared everyone against.
Source

Questions about rs61753391

What is rs61753391?

rs61753391 is a single position in the genome, in or near the DNAJC6 gene. Published research associates it with c-reactive protein 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 rs61753391 linked to?

On MyGeneLog this position is linked to C-Reactive Protein Levels. The research behind each link, and its sources, are set out on that condition page.

Does having rs61753391 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 rs61753391 come from?

GWAS Catalog, Nature genetics 2021, PMID:33462484. 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.

C-reactive protein levels (rs61753391). MyGeneLog™. https://www.mygenelog.com/variants/rs61753391

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