Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs17401966
rs17401966
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
A 0.900 GeneticVariation GWASDB We identified one intronic SNP (rs17401966) in KIF1B on chromosome 1p36.22 that was highly associated with HBV-related HCC and confirmed this association in five additional independent samples, consisting of 1,962 individuals with HCC, 1,430 control subjects and 159 family trios. 20676096

2010

dbSNP: rs17401966
rs17401966
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
A 0.900 GeneticVariation GWASCAT We identified one intronic SNP (rs17401966) in KIF1B on chromosome 1p36.22 that was highly associated with HBV-related HCC and confirmed this association in five additional independent samples, consisting of 1,962 individuals with HCC, 1,430 control subjects and 159 family trios. 20676096

2010

dbSNP: rs17401966
rs17401966
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
0.900 GeneticVariation BEFREE We identified one intronic SNP (rs17401966) in KIF1B on chromosome 1p36.22 that was highly associated with HBV-related HCC and confirmed this association in five additional independent samples, consisting of 1,962 individuals with HCC, 1,430 control subjects and 159 family trios. 20676096

2010

dbSNP: rs17401966
rs17401966
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
0.900 GeneticVariation BEFREE None of the replication cohorts showed associations between rs17401966 and HBV-derived HCC. 22712471

2012

dbSNP: rs17401966
rs17401966
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
0.900 GeneticVariation BEFREE Binary logistic regression showed that rs17401966 was not statistically associated with the risk of HCC development in Thai chronic HBV patients (p-value=0.998, OR=1.00 and 95% CI=0.68-1.48). 23803045

2013

dbSNP: rs17401966
rs17401966
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
0.900 GeneticVariation BEFREE These findings demonstrate that the presence of the G allele at rs17401966 of the KIF1B gene may decrease the risk for HCC and suggest that KIF1B may play a critical role in the development of HCC. 23634229

2013

dbSNP: rs17401966
rs17401966
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
0.900 GeneticVariation GWASDB Genetic variants in STAT4 and HLA-DQ genes confer risk of hepatitis B virus-related hepatocellular carcinoma. 23242368

2013

dbSNP: rs17401966
rs17401966
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
0.900 GeneticVariation BEFREE This meta-analysis showed a significant association between KIF1B rs17401966 polymorphism and HCC. 24952890

2014

dbSNP: rs17401966
rs17401966
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
0.900 GeneticVariation BEFREE A moderate increase in differentiation was noted for rs2596542 (F st = 0.106) and rs17401966 (F st = 0.116), single nucleotide polymorphisms (SNPs) associated with an increased risk of HCC in patients with chronic HCV and HBV, respectively. 24357186

2014

dbSNP: rs17401966
rs17401966
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
0.900 GeneticVariation BEFREE The SNP rs17401966 was genotyped using the TaqMan allelic discrimination assay in 414 intermediate or advanced hepatocellular carcinoma patients. 25153661

2014

dbSNP: rs17401966
rs17401966
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
0.900 GeneticVariation BEFREE Homozygous mutation of rs1081432 conferred a 2.68-fold risk of HCC (95% CI 1.35-5.34); however heterozygosity was not statistically significant. rs17401966 heterozygosity or homozygosity was not significantly associated with a increased risk of HCC. 25412941

2014

dbSNP: rs17401966
rs17401966
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
0.900 GeneticVariation BEFREE The gene-environment interaction between the KIF1B rs17401966 variant and alcohol consumption may contribute to the development of HCC in Chinese individuals. 27122668

2016

dbSNP: rs17401966
rs17401966
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
0.900 GeneticVariation BEFREE This meta-analysis suggested that KIF1B (rs17401966) polymorphism could decrease HCC risk in Chinese and in overall population, but not in non-Chinese. 29881295

2018

dbSNP: rs17401966
rs17401966
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
0.900 GeneticVariation BEFREE More well-designed studies with larger sample size and various ethnic groups and risk factors are needed to establish that KIF1B rs17401966 polymorphism is significantly associated with risk of HCC. 30947687

2019