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. 2020 Jun 10;45(2):241–250. doi: 10.4093/dmj.2019.0204

Table 2.

The interaction SNP pairs identified for type 2 diabetes mellitus

SNP pair Chr Positiona Geneb Allelec GENEVA
IPM
Combined P valued
MAF CR OR (95% CI) P value MAF CR OR (95% CI) P value
rs4947941 7 54871175 RP11-745C15.2 T/C 0.443 1 1.00 (0.98–1.02) 0.824 0.424 1 0.97 (0.92–1.02) 0.831 0.911
rs7785013 7 55152667 EGFR A/G 0.158 0.999 1.00 (0.98–1.03) 0.830 0.137 0.999 0.98 (0.91–1.05) 0.977 0.998
rs494794×rs7785013 - - - - - - 0.91 (0.88–0.95) 9.41×10−7 - - 0.78 (0.70–0.86) 1.73×10−6 4.84×10−10

SNP, single nucleotide polymorphism; Chr, chromosome; GENEVA, Gene Environment Association Studies initiative in Type 2 Diabetes; IPM, Biobank Program of the Institute of Personalized Medicine; MAF, minor allele frequency; CR, call rate; OR, odds ratio; CI, confidence interval; EGFR, epidermal growth factor receptor.

a

Position was relative to the hg19 version of the human genome,

b

The physical location of identified SNP,

c

The former allele represents the minor allele,

d

Meta-analyses results by using two genome-wide association study samples.