Table 4.
Per-allele association with 1 SD change in natural log-transformed NT-proBNP concentrations* | |||||||
---|---|---|---|---|---|---|---|
SNP | Chr | Position | Minor/Major Allele | MAF† | Quality Score | Beta (standard error) | P-Value |
rs198358‡ | 1 | 11826663 | C/T | 0.236 | N/A | 0.0829 (0.0680) | 0.228 |
rs5068 | 1 | 11828561 | G/A | 0.059 | 0.998 | −0.0035 (0.1255) | 0.978 |
rs632793 | 1 | 11833264 | G/A | 0.409 | 0.962 | 0.2012 (0.0631) | 0.0015 |
rs198389 | 1 | 11841858 | G/A | 0.427 | 0.987 | 0.1860 (0.0620) | 0.0029 |
Abbreviations: SNP, single nucleotide polymorphism; Chr, chromosome; MAF, minor allele frequency; SD, standard deviation.
Adjusted for Age, BMI, and systolic blood pressure. The mean (SD) natural logarithm transformed NT-proBNP concentration in the reference subcohort is 4.254 (0.821).
Minor allele frequency in the participants of European descent with available genotyping information and NT-proBNP concentrations. rs198358 was directly genotyped; genotyping information for the remaining SNPs was imputed.
This test of association used directly measured genotypes. The results did not differ when missing genotypes at rs198358 (n=1, or 0.22%) were replaced with the imputed estimated genotype dose.