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Table 2 Association analysis results of SNPs with suggestive genome-wide significance

From: A genome-wide analysis in cluster headache points to neprilysin and PACAP receptor gene variants

Index SNP

Position

Other SNPs in clump

Gene

A 1

A 2

A1-F case/controls

A1-F 1000G_all (1000G_EUR)a

P-value

OR (95% CI)

rs1006417

14:41803291

rs1782180, rs1779522, rs1778408, rs11157219, rs715334, rs12433558

 

G

A

0.11/0.26

0.19 (0.19)

1.40 × 10−6

0.34 (0.21–0.55)

rs12668955

7:31116168

 

ADCYAP1R1

G

A

0.34/0.52

0.55 (0.50)

9.10 × 10−6

0.48 (0.34–0.66)

rs1495452

3:65834076

 

MAGI1

A

G

0.55/0.38

0.39 (0.45)

1.43 × 10−5

2.03 (1.48–2.79)

rs2182605

1:117463537

 

PTGFRN

G

A

0.32/0.50

0.51 (0.48)

1.80 × 10−5

0.49 (0.35–0.68)

rs16895584

8:122518935

  

A

G

0.24/0.04

0.070 (0.054)

1.85 × 10−5

3.50 (2.03–6.02)

rs6469999

8:122415207

rs13255877, rs7833779

 

A

G

0.31/0.17

0.46 (0.16)

2.16 × 10−5

2.23 (1.56–3.19)

rs1509957

10:64610718

rs224308, rs10822065

 

G

A

0.60/0.43

0.43 (0.49)

2.66 × 10−5

1.99 (1.44–2.74)

  1. Abbreviations: A1 minor allele in study sample, A2 major allele, A1-F A1 frequency, OR odds ratio for minor allele, CI confidence interval
  2. aAllele 1 frequency in 1000 Genomes phase 3, all populations (1000G_all) and european population (1000G_EUR)