Skip to main content

Table 2 Phenotype associations for rs1244787406 (19:35 901 079 T > G) in FinnGen

From: Monoallelic TYROBP deletion is a novel risk factor for Alzheimer’s disease

 

OR (95% CI)

P-value

AF case

AF control

Dementia, including primary healthcare outpatient registry

2.10 (1.74–2.52)

3.29e- 15

0.0039

0.0025

Dementia

2.14 (1.77–2.59)

4.91e- 15

0.0039

0.0025

Unspecific neurodegenerative disorder

2.20 (1.81–2.68)

9.75e- 15

0.0042

0.0025

Any dementia

2.20 (1.81–2.68)

4.76e- 14

0.0040

0.0025

Alzheimer’s disease

2.36 (1.87–2.99)

3.01e- 13

0.0045

0.0025

  1. AF Allele frequency