Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs11614913
rs11614913
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.050 GeneticVariation BEFREE These findings underline the importance of the SNP rs11614913 for LSCC development in the Polish population and moreover highlight the different genetic background of the two studied neoplasms of the head and neck region. 29705927

2018

dbSNP: rs11614913
rs11614913
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.050 GeneticVariation BEFREE Patients who received donor livers with the rs11614913 homozygous CC variant presented significantly higher recurrence rates of HCC (41.7 vs. 15.3%, p = 0.009) and lower cumulative tumor-free survival (p = 0.005) than those who received TT wild-type donor livers. 26365437

2016

dbSNP: rs11614913
rs11614913
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.050 GeneticVariation BEFREE In this study, we examined 114 paired samples (tumor and normal tissues) from breast cancer patients to study the genotype distribution and somatic mutation of the SNP in MIR 196A2 (rs11614913 C-T). 26710106

2016

dbSNP: rs11614913
rs11614913
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.050 GeneticVariation BEFREE However, rs2910164 GG and rs11614913 CC genotypes and the rs2910164C/rs11614913C and rs2910164G/rs11614913C haplotypes were significantly overrepresented in PC patients with T1 and T2 tumor status than in those with T3 and T4. 23719600

2014

dbSNP: rs11614913
rs11614913
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.050 GeneticVariation BEFREE However, in a subsequent analysis of the association between this polymorphism and clinicopathological characteristics, there was an association between rs11614913 genotype and tumour size (p=0.046), but not with tumour number, grade, stage, invasiveness or Child-Pugh grade. 21080878

2010