Skip to main content

Table 3 In silico predicted functional effects of 7 non-coding SNPs in the pharmacogenetics of sulfonylureas treatment by Haploreg v4.1, RegulomeDB, and Ensembl’s VEP*

From: KCNJ11, ABCC8 and TCF7L2 polymorphisms and the response to sulfonylurea treatment in patients with type 2 diabetes: a bioinformatics assessment

SNP ID

Gene Symbol

dbSNP ID

SNP Location

Chromosome Location (GRCh38.p7)

HaploReg v4.1

Motifs changed by SNP

RegulomeDB Score/Prediction

Ensembl’s VEP

SNP37

KCNJ11

rs5210

3’-UTR

11:17386704

None

4/Minimal binding evidence

NA

SNP38

ABCC8

rs1799854

Intron 15

11:17427157

4 altered motifs

5/Minimal binding evidence

NA

SNP39

TCF7L2

rs7895340

Intron 5

10:113041766

Irf, PRDM1

NA

NA

SNP40

TCF7L2

rs7901695

Intron 4

10:112994329

None

5/Minimal binding evidence

NA

SNP41

TCF7L2

rs7903146

Intron 4

10:112998590

7 altered motifs

5/Minimal binding evidence

Risk factor

SNP42

TCF7L2

rs11196205

Intron 5

10:113047288

SMC3

5/Minimal binding evidence

Risk factor

SNP43

TCF7L2

rs12255372

Intron 5

10:113049143

5 altered motifs

NA

Risk factor

  1. *Abbreviations: RegulomeDB Regulome Database, SNP Single Nucleotide Polymorphism, UTR Untranslated Region, VEP Variant Effect Predictor, NA Not Available