Benign neoplasm: Stomach

CD2_BENIGN_STOMACH

Endpoint definition

Endpoint definition steps

FinnGen

Phenotype data

473681

1. Apply sex-specific rule

None

473681

2. Check conditions

None

473681

3. Check pre-conditions, main-only, mode, registry filters

Registry filters:

  • Hospital discharge: ICD-10 D13.1&
  • Hospital discharge: ICD-9 2111
  • Hospital discharge: ICD-8 2111
  • Cause of death: ICD-10 D13.1&
  • Cause of death: ICD-9 2111
  • Cause of death: ICD-8 2111

2 out of 7 registries used, show all original rules.

3330

4. Check minimum number of events

None

3330

5. Include endpoints

None

3330

6. Filter based on genotype QC (FinnGen only)

3226

Control definitions (FinnGen only)

Controls for this endpoint are individuals that are not cases.

Extra metadata

Level in the ICD hierarchy 3
First used in FinnGen datafreeze DF2
Parent code in ICD-10 D13
Name in latin Neoplasma benignum ventriculi

Case counts by codes

FinnGen case counts by registry codes:

generic upset plot

Upset plot

Full data table

Summary Statistics

-FinRegistry-

Key figures

All Female Male
Number of individuals
Whole population 19792 12427 7254
Only index persons 17931 11514 6417
Unadjusted period prevalence (%)
Whole population 0.30 0.36 0.20
Only index persons 0.36 0.42 0.24
Median age at first event (years)
Whole population 65.96 65.50 66.71
Only index persons 65.31 64.86 66.13

-FinnGen-

Key figures

All Female Male
Number of individuals 3226 2058 1168
Unadjusted period prevalence (%) 0.73 0.81 0.59
Median age at first event (years) 64.29 62.79 66.94

-FinRegistry-

Age distribution of first events

-FinnGen-

Age distribution of first events

-FinRegistry-

Year distribution of first events

-FinnGen-

Year distribution of first events

-FinRegistry-

Cumulative Incidence Function

-FinnGen-

Cumulative Incidence Function

Mortality – FinRegistry

Association

Association between endpoint CD2_BENIGN_STOMACH and mortality.

Females

Parameter HR [95% CI] p-value
CD2_BENIGN_STOMACH 1.275 [1.15, 1.41] < 0.001
Birth year 0.993 [0.98, 1.0] 0.086

During the follow-up period (1.1.1998 — 31.12.2019), 2054 out of 10219 females with CD2_BENIGN_STOMACH died.

Males

Parameter HR [95% CI] p-value
CD2_BENIGN_STOMACH 1.407 [1.25, 1.58] < 0.001
Birth year 0.987 [0.98, 1.0] 0.008

During the follow-up period (1.1.1998 — 31.12.2019), 1717 out of 5767 males with CD2_BENIGN_STOMACH died.

Mortality risk

Mortality risk for people of age

years, who have CD2_BENIGN_STOMACH.

N-year risk Females Males
1 0.146% 0.235%
5 0.713% 1.615%
10 1.746% 4.04%
15 3.232% 7.786%
20 5.547% 13.066%

Relationships between endpoints

Index endpoint: CD2_BENIGN_STOMACH – Benign neoplasm: Stomach

GWS hits: 2

Endpoint
Case Overlap
Survival Analysis
Genetic Correlations
Genetic Signals
N (Jaccard index)
HR [CI]
Extremity
rg [CI]
Extremity
Hits
Coloc Hits
FinRegistry
FinnGen
FinRegistry
FinnGen
FinnGen
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