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. 2017 Nov 14;103(1):125–138. doi: 10.1210/jc.2017-01531

Table 1.

Pleiotropic Loci Associated With Both FN BMD and BMI/WHR With cFDR <0.05

Characteristic rs3759579 rs2178950 rs1473 rs9825174 rs2047937 rs17277372 rs335170
Gene MARK3 TRPS1 PUM1 XXYLT1 ZNF423 DNM3 PRDM6
Chromosome 14q32.32 8q24.12 1p35.2 3q29 16q12 1q24.3 5q23.2
A1 A C A C C A A
A2 G G G T T G C
P value BMI 2.18E-05 8.86E-04 4.89E-04 7.13E-04 / / /
P value WHR / / / / 3.80E-04 1.60E-03 2.20E-03
P value FN BMD 3.31E-05 3.95E-04 2.67E-04 2.50E-04 2.10E-07 7.80E-07 1.80E-05
Effect for BMI + / / /
Effect for WHR / / / / + +
Effect for FN BMD + + +
cFDR BMI|FN BMD 7.43E-04 3.06E-02 2.66E-02 3.64E-02 / / /
cFDR FN BMD|BMI 3.54E-03 4.08E-02 4.33E-02 4.78E-02 / / /
cFDR WHR|FN BMD / / / / 1.14E-03 6.40E-03 1.91E-02
cFDR FN BMD|WHR / / / / 2.21E-05 1.01E-04 1.96E-03
ccFDR 3.54E-03 4.08E-02 4.33E-02 4.78E-02 1.14E-03 6.40E-03 1.91E-02

Independent gene loci (r2 < 0.2) with SNPs that have ccFDR <0.05 in FN BMD and BMI/FN BMD and WHR. All SNPs are listed with their nearest gene(s), chromosomal location, effect allele A1, noneffect allele A2, raw P values for univariate GWAS for each trait, cFDR values for each trait, and ccFDR values. The effect direction of the potentially pleiotropic SNP on FN BMD and BMI/WHR was obtained from the original GWAS data. The effect represents the summary of effect directions (“+” indicates positive effect of A1 allele, “−” indicates negative effect of the A1 allele, and “/” indicates there is no value for the column).