Table 2.
SNP | Gene | Chr | Position | MAF (%) | P value |
---|---|---|---|---|---|
rs74640812 | FRG2C: Missense Variant | 3 | 75,665,674 (GRCh38.p12) | 49.5 | 9.9×10−7 |
rs972925 | OR1Q1: Missense Variant | 9 | 122,614,808 (GRCh38.p12) | 7.5 | 2.5×10−6 |
rs60460416 | DNAH17: Intron Variant | 17 | 78,445,748 (GRCh38.p12) | 6 | 6.6×10−7 |
rs2289752 | DNAH17: Missense Variant | 17 | 78,450,295 (GRCh38.p12) | 5 | 4.8×10−6 |
Abbreviations: SNP, single-nucleotide polymorphism; Chr, chromosome; MAF, minor allele frequency.