SNP ID | SNP ID | SNP ID | SNP ID | SNP ID | SNP ID | SNP ID | SNP ID |
---|
rs11926701 | chr3:196,236,401 | A | 0.03 | 9.23E-09 | 6.70 (3.42–13.13) | SMCO1 | missense variant |
rs1130838 | chr6:31,237,124 | A | 0.13 | 5.81E-05 | 0.45 (0.29–0.68) | HLA-C | missense variant |
rs2279685 | chr15:34,649,631 | A | 0.26 | 5.81E-05 | 0.56 (0.42–0.75) | NUTM1 | missense variant |
- Results of Fisher's exact test showing SNPs with P-value < 1.0 × 10–4. The SNP ID and chromosomal position (BP) are based on NCBI genome build 37/hg19. Abbreviations are as follows: SNP single nucleotide polymorphism, chr chromosome, BP physical position (base-pair), MA minor allele, MAF minor allele frequency, OR Odd ratio, CI confidence interval