Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs4950928
rs4950928
CUI: C1269955
Disease: Tumor Cell Invasion
Tumor Cell Invasion
0.010 GeneticVariation BEFREE In 200 HBsAg negative HCC patients, we observed that the <i>CHI3L1</i> rs4950928 polymorphisms carriers with the variant genotype CG+GG had higher frequencies of vascular invasion. 28260989

2017