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. 2017 Jun 14;2017(1):hox002. doi: 10.1093/hropen/hox002

Table I.

An association analysis of the three SNPs with serum testosterone levels in two Japanese male cohorts.

SNP Chr Position Gene Location Effect/other Cohort 1 (N = 901) Cohort 2 (N = 786) Combined Heterogeneity
EAF βSTD (SE) P EAF βSTD (SE) P βSTD (SE) [model]a Pmeta Var (%)b Phetero I2 (%)
Testosterone
 rs2075230 17 7487108 SHBG Upst. A/G 0.565 0.18 (0.046) 1.3 × 10−4 0.556 0.12 (0.049) 1.4 × 10−2 0.15 (0.033) [F] 7.2 × 10−6 1.1 0.39 0.0
 rs6259 17 7536527 SHBG Exon A/G 0.107 0.073 (0.075) 0.33 0.116 0.26 (0.072) 3.8 × 10−4 0.17 (0.092) [R] 0.071 0.5 0.076 68.1
 rs727428 17 7537792 SHBG Dwnst. G/A 0.396 0.11 (0.048) 0.019 0.366 0.050 (0.049) 0.31 0.082 (0.034) [F] 0.017 0.3 0.36 0.0

Data are shown as the estimated standardized linear regression statistic βSTD, SE and P value with adjustments for age and BMI. Testosterone and sex hormone-binding globulin (SHBG) were processed using natural log-transformed variables. Bold numbers indicate significance (P value < 0.0083) after adjusting for multiple testing. SNP, single nucleotide polymorphisms; Chr, chromosome; EAF, effect allele frequency; βSTD, standardized regression coefficient; Phetero, P value for heterogeneity; Upst., upstream; Dwnst., downstream.

aThe β-coefficient and its SE were summarized using an inverse variance-weighted meta-analysis, under fixed-effects model [F] or the DerSimonian and Laird method under random-effects model [R].

bPercentage of phenotypic variance (log-transformed) explained by SNP.