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Standard

Revision surgery after total joint arthroplasty

CAMTA1 · rs11120968

Strength of the evidence

1 / 4

Its strongest genetic-study result is p = 10−8, with 1 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 94 cases from twins, 1,036 controls from twins.

The effect Each copy of the A allele carried 2.34 times the odds of Revision surgery after total joint arthroplasty (95% confidence interval 1.74-3.13); p = 1 × 10−8.

How common The A allele had a frequency of about 36% in the people studied.

Where it sits Chromosome 1, band 1p36.23 — in an intron of CAMTA1.

How common each version is

AG
Korean KRGDB
A 30.2% · G 69.8%
Korean Korea4K
A 29.0% · G 71.0%
Korean Korea1K
A 27.8% · G 72.2%
Japanese ToMMo
A 27.6% · G 72.4%
Vietnamese
A 21.3% · G 78.7%
World gnomAD
A 36.1% · G 63.9%
World 1000 Genomes
A 33.7% · G 66.3%
World TOPMed
A 35.8% · G 64.2%

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.

What each result means

A/A Two copies of the version the research linked to Revision surgery after total joint arthroplasty. 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 Revision surgery after total joint arthroplasty. That is a smaller link than two copies.
G/G No copy of the version the research linked to Revision surgery after total joint arthroplasty. This is the starting point the study compared everyone against.
Source

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Revision surgery after total joint arthroplasty (rs11120968). MyGeneLog™. https://www.mygenelog.com/variants/rs11120968

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