Research Article

Functional Analysis of the Coronary Heart Disease Risk Locus on Chromosome 21q22

Table 1

The association between four SNPs at the CHD risk locus on chromosome 21q22 and mean QT interval in UCLEB.

SNPBeta coefficient value

rs9982601GenotypeCCTCTT1.83 (0.90)0.04
(frequency)5329 (0.75)1643 (0.23)130 (0.02)
Mean QT interval (ms)402.8 (37.35)404.5 (39.28)409.1 (41.08)

rs8131284GenotypeTTCTCC2.14 (0.89)0.02
(frequency)5293 (0.75)1670 (0.24)142 (0.02)
Mean QT interval (ms)402.7 (37.41)404.9 (39.20)408.1 (38.97)

rs7278204GenotypeAAGAGG2.07 (0.89)0.02
(frequency)5290 (0.74)1673 (0.24)141 (0.02)
Mean QT interval (ms)402.7 (37.73)404.9 (38.19)407.9 (39.26)

rs973754GenotypeAAGAGG1.85 (0.89)0.02
(frequency)5300 (0.75)1663 (0.23)142 (0.02)
Mean QT interval (ms)402.7 (37.75)404.6 (38.18)408.2 (38.84)

Mean QT interval is shown by genotype as well as the beta coefficient (±standard deviation) for the minor allele at each SNP.