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Table 2 CNV association results with p-values <0.01 for FPG and FPI

From: Genome-wide copy number variation analysis identified deletions in SFMBT1 associated with fasting plasma glucose in a Han Chinese population

Trait/CNV/SNP

Chrom

Position

Gene

Freqa

P-value

Adj-Pb

FDR

FPG

 Deletion

   rs2336721 c

3

53,003,415

SFMBT1

0.052

0.0002

0.0478

0.0669

   rs2581795

3

53,013,826

SFMBT1

0.052

0.0002

0.0478

0.0669

FPI

 Deletion

  rs11209948

1

72,584,492

None

0.106

0.0020

0.2442

0.4583

  rs2815752

1

72,585,028

None

0.090

0.0030

0.2240

0.4657

  rs3931686

12

9,533,761

None

0.121

0.0042

0.3332

0.8368

 Duplication

  rs1823636

11

4,232,580

None

0.072

0.0038

0.0776

0.1593

  rs438821

11

4,232,709

None

0.072

0.0038

0.0776

0.1593

  rs11031481

11

4,252,795

None

0.069

0.0070

0.1212

0.1910

  1. aCNV frequency
  2. bPermutation adjusted p-value for multiple testing
  3. cResults with adjusted p-value <0.05 were marked as bold