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Table 1 The 12 SNPs in the five genes evaluated in this cohort study

From: Unique genetic variants of lean nonalcoholic fatty liver disease: a retrospective cohort study

Gene

SNP IDa

Alleles

Chromosomeb

Function

FTO

rs1421085

T/C

16:53,767,042

intron variant

FTO

rs3751812

G/T

16:53,784,548

intron variant

FTO

rs8050136

C/A

16:53,782,363

intron variant

FTO

rs9939609

T/A

16:53,786,615

intron variant

TFAP2B

rs2206277

C/T

6:50,830,813

intron variant

TBC1D1

rs2279027

T/A

4:37,902,135

missense variant

TBC1D1

rs2279026

T/C

4:37,902,461

synonymous variant

TBC1D1

rs2279028

A/C

4:37,902,048

genic upstream transcript variant

GCKR

rs780093

T/C

2:27,519,736

intron variant

GCKR

rs780094

T/C

2:27,518,370

intron variant

GCKR

rs1260326

T/C

2:27,508,073

missense variant

KCNJ11

rs5215

C/T

11:17,387,083

missense variant

  1. aAccording to the dbSNP database
  2. bThe SNP Chromosome positions are based on the NCBI human genome