Gene: ANGPTL8 ×
Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2278426
rs2278426
ANGPTL8 ; DOCK6
0.030 GeneticVariation BEFREE The rates of T2D and IGT were greater in subjects with the R59W variant. 29397342

2019
dbSNP: rs2278426
rs2278426
ANGPTL8 ; DOCK6
0.030 GeneticVariation BEFREE Our results suggest that the rs2278426 (C/T) variant is associated with increased risk of T2DM and may cause dyslipidemia due to its effect on decreasing HDL-C levels. 30191588

2019
dbSNP: rs2278426
rs2278426
ANGPTL8 ; DOCK6
0.030 GeneticVariation BEFREE Interaction between endothelial nitric oxide synthase rs1799983, cholesteryl ester-transfer protein rs708272 and angiopoietin-like protein 8 rs2278426 gene variants highly elevates the risk of type 2 diabetes mellitus and cardiovascular disease. 29973202

2018
dbSNP: rs892066
rs892066
ANGPTL8 ; DOCK6
0.010 GeneticVariation BEFREE Genotype and allele distribution of rs892066 (C/G) was not statistically significant in T2DM patients compared to the control group. 30191588

2019
dbSNP: rs145464906
rs145464906
ANGPTL8 ; DOCK6
0.010 GeneticVariation BEFREE We found no significant association of p.Q121X with either fasting glucose or type 2 diabetes (p-value = 0.90 and 0.65, respectively). 26822414

2016