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Table 5 Influence of common variants in HNF1A target genes on age at diagnosis

From: Variants influencing age at diagnosis of HNF1A-MODY

Gene

SNP ID

Effective allele

Est. G

Est. G:D domain

Est. G:T domain

GxE p-value

AFP/AFM

rs12510870

C

− 0.0658

0.0782

0.1418

0.0096

rs16849364

G

− 0.0472

0.0322

0.1290

0.0218

rs4640638

G

− 0.0437

0.0449

0.1211

0.0355

CYP1A2

rs12441817

C

0.0228

− 0.4899

− 0.0044

0.0109

SLCO1B3

rs10841644

C

− 0.0049

0.2745

0.0089

0.0089

rs7965380

C

− 0.0019

0.2716

0.0073

0.0097

rs957164

G

0.0031

0.2797

− 0.0138

0.0103

rs2033515

G

− 0.0406

0.3366

0.0458

0.0193

MTTP

rs12647527

G

− 0.0063

− 0.1420

0.0376

0.0050

rs881980

G

− 0.0025

− 0.4047

0.0365

0.0094

CRP

rs12094103

G

0.01945

− 0.2369

− 0.0718

0.0115

rs3122012

C

0.0116

− 0.2509

− 0.0597

0.0123

CSRP1

rs7525711

G

− 0.0186

− 0.2557

0.0517

0.0063

rs11577209

G

− 0.0115

− 0.1766

0.0833

0.0111

rs10920205

G

− 0.0061

− 0.2557

0.0100

0.0139

rs2038972

C

− 0.0466

0.0086

0.1344

0.0286

  1. D dimerization domain, HNF1A hepatocyte nuclear factor-1-alpha, ID identifier, SNP single-nucleotide polymorphism, T transactivation domain, Est G. main effect of the risk allele estimated in the Linear Mixed Model; Est G:D the estimated interaction effect of the risk allele and the indicator variable of the dimerization domain; Est G:T the estimated interaction effect of the risk allele and the indicator variable of the transactivation domain; GxE p-value: the p-value for the null hypothesis that the Est G:T and Est G:D equal zero; Joint p-value the p-value for the null hypothesis that Est G, Est G:T and Est G:D equal zero