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Table 4 Colocalization analysis results for exposures instrumented through only one SNP

From: A phenome-wide approach to identify causal risk factors for deep vein thrombosis

Analysis type

Exposure

nr SNP*

PP.H0

PP.H1

PP.H2

PP.H3

PP.H4

BMI-associated proteins

Plasminogen activator inhibitor 1

2604

3.0254E-13

1.9614E-06

3.9637E-09

0.02472248

0.97527556

Neurogenic locus notch homolog protein 1

3856

1.0694E-79

4.778E-73

2.2382E-07

0.99999972

6.0801E-08

Inhibin beta C chain

4079

1.1109E-29

2.6137E-23

4.2502E-07

0.99999948

9.3591E-08

MR-PheWAS

Lysine

547

2.4588E-11

0.98338278

3.2772E-13

0.01310352

0.0035137

Bipolar disorder / mania

3533

0.47264348

0.43702738

0.03965284

0.03665077

0.01402554

Chronic obstructive pulmonary disorder

4229

0.0766326

0.83975957

0.00333097

0.03645779

0.04381907

X-14473

655

6.292E-07

0.83967623

6.959E-08

0.09280245

0.06752062

Docosapentaenoate

614

1.9077E-08

0.62830917

1.1181E-09

0.03649044

0.33520037

Adrenate

626

1.8886E-18

0.5838098

1.1167E-19

0.03413747

0.38205274

Stearidonate

674

5.34E-11

0.50441818

3.2335E-12

0.03007888

0.46550294

Eicosapentanoate

633

2.8064E-17

0.22721212

1.6606E-18

0.01268473

0.76010315

Arachidonate

626

4.9721E-77

0.17796851

2.9399E-78

0.00971061

0.81232088

  1. Posterior probabilities for: H0 (no causal variant), H1 (causal variant for trait 1 only), H2 (causal variant for trait 2 only), H3 (two distinct causal variants) and H4 (one common causal variant)
  2. *nr SNPs are the number of SNPs in the 500 kb genomic window used to run the colocalization analysis