Table 2.
Chromosome (position) | SNP ID | MAF | Minor allele | GWAS Effect Size, Best Analysis | GWAS SE, Best Analysis | GWAS P value, Best Analysis | Ancestries/ Diagnosis/ Model for Best Analysis | Nearest Gene(s) | Replication Beta | Replication SE | Replication P Value | Meta- analysis Beta | Meta- analysis SE | Meta- analysis P Value |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Associations from primary analysis with P < 5 × 10 –7 | ||||||||||||||
3 (118950499) | rs7628585 | 0.182 | A | 0.338 | 0.0621 | 5.54E-08 | Primary analysis | B4GALT4 | –0.091 | 0.181 | 6.17E-01 | 0.292 | 0.059 | 6.47E-07 |
1 (235531451) | rs1977748 | 0.411 | T | –0.286 | 0.0563 | 3.75E-07 | Primary analysis | TBCE | 0.001 | 0.159 | 9.96E-01 | –0.254 | 0.053 | 1.72E-06 |
Associations from secondary analyses with P < 5 × 10 –8 | ||||||||||||||
1 (10194439) | rs55704135 | 0.03 | A | –0.934 | 0.159 | 4.24E-09 | European/all/ maximum | UBE4B | –0.231 | 0.308 | 4.54E-01 | –0.786 | 0.141 | 2.65E-08 |
3 (98383646) | rs189532746 | 0.013 | A | –1.635 | 0.282 | 6.95E-09 | All/ISS/ minimum | CPOX, ST3GAL6 | NP | NP | NP | NP | NP | NP |
12 (10300486) | rs78263566 | 0.025 | G | 1.685 | 0.283 | 8.50E-09 | European/ GHD/ maximum | CLEC7A, OLR1 | 0.182 | 0.721 | 8.01E-01 | 1.485 | 0.2631 | 1.67E-08 |
8 (98853066) | rs74523128 | 0.01 | A | 2.516 | 0.430 | 1.52E-08 | European/ GHD/ maximum | LAPTM4B | ND | ND | ND | ND | ND | ND |
6 (116512418) | rs144751704 | 0.014 | T | –1.299 | 0.232 | 2.12E-08 | European/all/ minimum | NT5DC1/ COL10A1 | NP | NP | NP | NP | NP | NP |
Chromosome and position are based on the hg37 build of the human genome. Best analysis refers to the ancestry/diagnosis/model with the best P value in the GWAS for that variant. Replication and meta-analysis results are shown for that best analysis.
Abbreviations: GWAS, genome-wide association study; MAF, minor allele frequency; ND, not done; NP, not polymorphic; SNP, single nucleotide polymorphism.