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Table 2 Top 10 genetic markers associated with CFS based on weighted genetic variation (WGV) estimated by the Bayesian model

From: Prediction of complex human diseases from pathway-focused candidate markers by joint estimation of marker effects: case of chronic fatigue syndrome

SNP ID

Proxy SNP

Gene symbola

SNP annotationa

WGV

SE of WGVb

rs2288831

rs3212227

IL12B

Intron (UTR-3)

3.95

0.0299

rs2071376

 

IL1A

intron

3.6

0.0296

rs2069718

 

IFNG

intron

3.34

0.0272

rs846906

 

HSD11B1

intron

3.29

0.0337

rs1923884

 

HTR2A

intron

3.16

0.0324

rs1799836

 

MAOB

Intron

2.56

0.0394

rs363236

rs3814230

SLC18A2 (PDZD8)

UTR-3 (synonymous codon)

2.31

0.0272

rs1396862

rs1218523

CRHR1 (IMP5)

Intron (missense codon)

2.31

0.0334

rs891512

rs743507

NOS3

Intron

2.18

0.0287

rs1124492

rs46220755

DRD2

Intron

2.02

0.0312

  1. aGene symbol and SNP annotation in parenthesis correspond to proxy SNPs, if different from the genotyped SNPs for the model
  2. bSE of WGV standard error of weighted genetic variation