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Table 1 Functional loci for colorectal cancer detected from exome array association analysis

From: Identification and functional validation of HLA-C as a potential gene involved in colorectal cancer in the Korean population

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

  1. 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