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 |