This is a non-core endpoint: only basic statistics are computed.
See these related core endpoints for full statistics:
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This is a non-core endpoint: only basic statistics are computed.
See these related core endpoints for full statistics:
CD2_BENIGN_VERTEB_COLUMN
No definition available.
Endpoint definition steps |
FinnGen |
---|---|
Phenotype data |
520210 |
1. Apply sex-specific ruleNone |
520210 |
2. Check conditionsNone |
520210 |
3. Check pre-conditions, main-only, mode, registry filtersRegistry filters:
2 out of 7 registries used, show all original rules. |
88 |
4. Check minimum number of eventsNone |
88 |
5. Include endpointsNone |
88 |
6. Filter based on genotype QC (FinnGen only) |
88 |
Control definitions (FinnGen only)
Controls for this endpoint are individuals that are not cases.
Extra metadata
List of similar endpoints to Benign neoplasm: Vertebral column based on the number of shared cases.
Similar with more cases:
Similar with less cases:
This endpoint is excluded from FinRegistry analyses (omitted endpoint).
All | Female | Male | |
---|---|---|---|
Number of individuals | 88 | 46 | 42 |
Unadjusted period prevalence (%) | 0.02 | 0.02 | 0.02 |
Median age at first event (years) | 52.69 | 49.76 | 55.89 |
Not a core endpoint, no data to show.
CodeWAS is a tool for exploring the associations between an endpoint and all of the medical codes and drug codes.
This is a new tool, please reach out using the contact form for feedback and improvement ideas.
First, a cohort is built by matching controls to the endpoint cases using year of birth and sex. Then, a Fisher test is done for all the medical codes and drug codes between the cases and controls of this cohort. Codes are reported in the table below if they have −log10(p-value) ≥ 6.
This endpoint is excluded from FinRegistry analyses (omitted endpoint).
Index endpoint: CD2_BENIGN_VERTEB_COLUMN – Benign neoplasm: Vertebral column
GWS hits: -
This endpoint is excluded from FinRegistry analyses (omitted endpoint).