Endpoint definition
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FinnGen phenotype data
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First used in FinnGen datafreeze
DF2
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List of similar endpoints to
Hypothyroidism (congenital or acquired)
based on the number of shared cases.
Broader endpoints:
Narrower endpoints:
| All | Female | Male | |
|---|---|---|---|
| Number of individuals | 32920 | 26357 | 6563 |
| Unadjusted prevalence (%) | 12.66 | 17.94 | 5.80 |
| Mean age at first event (years) | 52.18 | 50.79 | 57.79 |
| Follow-up | Absolute risk | HR [95% CI] | p | N |
|---|---|---|---|---|
| 1998–2019 | 0.02 | 1.48 [1.28, 1.71] | 6.5e-8 | 2141 |
| 15 years | 0.01 | 1.70 [1.50, 1.92] | 4.7e-17 | 1708 |
| 5 years | 0.00 | 2.33 [2.06, 2.65] | 3.2e-39 | 621 |
| 1 year | 0.00 | 1.89 [1.48, 2.41] | 2.8e-7 | 92 |
Index endpoint: HYPOTHYROIDISM – Hypothyroidism (congenital or acquired)
GWS hits: 38
before Hypothyroidism (congenital or acquired)
after Hypothyroidism (congenital or acquired)
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