Table 2.
SNP | Locus | Location | CHR | N | EA | B (SE) | p value |
---|---|---|---|---|---|---|---|
rs11708067 | ADCY5 | Intron | 3 | 358 | A | − 0.90 (0.38) | 0.019 |
rs340874 | PROX1 | Intergenic | 1 | 305 | C | 0.09 (0.15) | 0.56 |
rs560887 | G6PC2/ABCB11 | Intron | 2 | 303 | C | 0.027 (0.13) | 0.83 |
rs10885122 | ADRA2A | Intergenic | 10 | 313 | G | − 0.075 (0.37) | 0.84 |
rs4607517 | GCK | Intergenic | 7 | 340 | A | − 0.005 (0.17) | 0.98 |
rs2191349 | DGKB/TMEM195 | Intergenic | 7 | 368 | T | − 0.07 (0.20) | 0.72 |
rs7034200 | GLIS3 | Intron | 9 | 342 | A | − 0.04 (0.19) | 0.82 |
rs7944584 | MADD | Intron | 11 | 303 | A | − 0.24 (0.28) | 0.40 |
rs174550 | FADS1 | Intron | 11 | 304 | T | − 0.001 (0.13) | 0.99 |
rs10830963 | MTNR1B | Intron | 11 | 314 | G | 0.12 (0.18) | 0.49 |
rs11605924 | CRY2 | Intron | 11 | 365 | A | − 0.60 (0.32) | 0.064 |
rs7756992 | CDKAL1 | Intron | 6 | 313 | G | − 0.25 (0.20) | 0.21 |
SNP = single nucleotide polymorphism, CHR = chromosome, EA = effect allele, B = beta/effect size, SE = standard error; N = number of women with successful genotyping