Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1384565
rs1384565 		0.010 GeneticVariation BEFREE <b>Results:</b> We found both rs1384565 CC genotype (12.1 compared with 6.6%, <i>P</i><0.001) and C allele (35.2 compared with 24.4%, <i>P</i><0.001) were more frequent in the T2DM patients than in the controls. 30413610

2018