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Table 2 Genotype-specific means for single cross-sectional HbA1c levels in 1,486 subjects with type 2 diabetes.

From: Evaluation of four novel genetic variants affecting hemoglobin A1c levels in a population-based type 2 diabetes cohort (the HUNT2 study)

Nearest gene

SNP

Common homozygote

Heterozygote

Rare homozygote

Minor allele*

Major allele*

MAF

MISS #

  

N

Mean

SD

N

Mean

SD

N

Mean

SD

    

BNC2

rs10810632

1215

8.05

0.52

257

8.12

0.11

13

7.95

0.65

C

T

0.09

1

SORCS1

rs1358030

648

7.94

0.07

622

8.16

0.07

139

8.02

0.16

C

T

0.32

77

GSC

rs11624318

908

8.07

0.06

500

8.02

0.08

76

8.11

0.21

A

C

0.22

2

WDR72

rs566369

1218

8.02

0.05

251

8.18

0.12

10

8.89

0.74

A

G

0.09

7

  1. Risk alleles are defined according to Paterson et al. [20], and underlined and highlighted in bold.
  2. MAF = minor allele frequency
  3. MISS# = number of individuals with missing genotype data
  4. * Alleles are indexed from the forward strand of the human reference sequence NCBI Build 36.
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BMC Medical Genetics

ISSN: 1471-2350

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