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Table 1 Results for loci reaching genome-wide significance in the multi-phenotype rare variant analysis of NFBC1966 (N = 4,721). Regression coefficients with their standard errors (SE) are reported, followed by the P-value and the Bayesian Information Criterion (BIC) for the analysed model. TG, triglycerides; ln(FI), natural logarithm transformed fasting insulin; WHR, waist-to-hip ratio

From: MARV: a tool for genome-wide multi-phenotype analysis of rare variants

 

APOA5

(Chr 11: 116,660,086-116,663,136)

ZNF259

(Chr 11: 116,649,276-116,658,739)

Model

β (SE)

P-value; BIC

β (SE)

P-value; BIC

TG + ln(FI) + WHR, full model a

 

3.32 × 10−8; −19877.3

 

6.3 × 10−8; −25069.6

 TG

0.011 (0.002)

-

0.007 (0.001)

-

 ln(FI)

−0.010 (0.004)

-

−0.008 (0.002)

-

 WHR

0.027 (0.019)

-

0.010 (0.011)

-

TG + ln(FI)

 

2.00 × 10−8; −19883.5

 

1.8 × 10−9; −25077.3

 TG

0.011 (0.002)

-

0.007 (0.001)

-

 ln(FI)

−0.010 (0.004)

-

−0.007 (0.002)

-

TG + WHR

 

3.34 × 10−7; −19877.9

 

4.1 × 10−7; −25066.5

 TG

0.009 (0.002)

-

0.005 (0.001)

-

 WHR

0.020 (0.019)

-

0.005 (0.001)

-

ln(FI) + WHR

 

0.08; −19853.1

 

0.10; −25427.6

 ln(FI)

−0.003 (0.004)

-

−0.003 (0.002)

-

 WHR

0.041 (0.019)

-

0.019 (0.011)

-

Univariate b

 TG

0.009 (0.002)

9.15 × 10−8; −19885.1

0.005 (0.001)

6.5 × 10−8; −25074.7

 ln(FI)

−0.002 (0.003)

0.62; −19856.8

−0.002 (0.002)

0.27; −25046.7

 WHR

0.038 (0.019)

0.04; −19860.7

0.016 (0.011)

0.16; −25047.5

  1. a For a genome-wide joint analysis, the level of significance is P < 1.67 × 10−6 after Bonferroni correction for 30,000 genes
  2. b For univariate analysis, the level of significance is P < 5.56 × 10−7 after Bonferroni correction for 30,000 genes and three phenotypes