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Table 3 FDR BH adjustment

From: Susceptible gene polymorphism in patients with three-vessel coronary artery disease

Allele model

Gene

SNP

P-value

Q-value

Dominant model

CDKN2B-AS1

rs1333049

0.001

0.009

CDKN2B-AS1

rs1333042

0.001

0.009

CDKN2B-AS1

rs10757274

0.001

0.009

CDKN2B-AS1

rs4977574

0.001

0.009

CDKN2B-AS1

rs9632884

0.002

0.009

CDKN2B-AS1

rs3217986

0.018

0.054

CDKN2B-AS1

rs1063192

0.022

0.0495

Recessive model

CDKN2B-AS1

rs1333049

0.004

0.036

CDKN2B-AS1

rs4977574

0.008

0.036

CDKN2B-AS1

rs10757274

0.008

0.036

Codominant model

CDKN2B-AS1

rs1333049

0.001

0.009

CDKN2B-AS1

rs4977574

0.001

0.009

CDKN2B-AS1

rs10757274

0.001

0.009

CDKN2B-AS1

rs9632884

0.004

0.018

CDKN2B-AS1

rs1333042

0.004

0.018

CDKN2B-AS1

rs3217986

0.023

0.069

  1. FDR BH false discovery rate Benjamini-Hochberg
  2. Q-value = P-value*number of hypothesis testing/rank of P-value
  3. Number of hypothesis testing = number of SNPs detected on one gene