Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs895819
rs895819
0.100 GeneticVariation BEFREE To explore the relevance of miRNA polymorphisms and female physiological characteristics to breast cancer risk, SNPs located within hsa-miR-605 (rs2043556), hsa-miR-149 (rs2292832), hsa-miR-27a (rs895819), hsa-miR-196a-2 (rs11614913) and hsa-miR-618 (rs2682818) were selected, and their associations with breast cancer risk were analysed. 22074121

2012

dbSNP: rs895819
rs895819
0.100 GeneticVariation BEFREE The findings suggest that pre-mir-27a rs895819 polymorphism may have some relation to breast cancer susceptibility or cancer development in Caucasian. 23266669

2013

dbSNP: rs895819
rs895819
0.100 GeneticVariation BEFREE These findings suggest that hsa-mir-27a rs895819 polymorphism may play an important role in breast cancer development. 23464432

2012

dbSNP: rs895819
rs895819
0.100 GeneticVariation BEFREE This meta-analysis suggests that the pre-miR-27a rs895819 polymorphism may contribute to the susceptibilities of some specific-type of cancers, including breast cancer, renal cell cancer, nasopharyngeal cancer and digestive tract cancers, as well as the susceptibilities of cancers in Caucasians to some extent. 23762318

2013

dbSNP: rs895819
rs895819
0.100 GeneticVariation BEFREE In conclusion, our results suggest that the SNP rs895819 may serve as a risk factor for breast cancer in younger Chinese populations; however, larger population-based studies are needed to validate these findings. 23954879

2013

dbSNP: rs895819
rs895819
0.100 GeneticVariation BEFREE Four breast cancer-related microRNA polymorphisms (miR-27aA > G [rs895819], miR-135bC > T [rs74141216], miR-423C > A [rs6505162], and miR-608G > C [rs4919510]) were genotyped in 136 women with idiopathic POI and 224 controls of Korean ethnicity using polymerase chain reaction-restriction fragment length polymorphism analysis. 25203895

2015

dbSNP: rs895819
rs895819
0.100 GeneticVariation BEFREE Our meta-analysis results suggested that the rs2910164 and rs3746444 polymorphisms are associated with increased BC risk, while the rs11614913 and rs895819 polymorphisms correlate with reduced BC risk. 25483824

2015

dbSNP: rs895819
rs895819
0.100 GeneticVariation BEFREE Further studies showed a significant association between the [G] allele of rs895819 and decreased risk of breast cancer (0.91; 95%CI, 0.85-0.98), and stratified analyses indicated a protective effect of the [G] allele in Caucasians (OR, 0.89; 95%CI, 0.82-0.98), younger breast cancer cases (OR, 0.87; 95%CI, 0.79-0.96), and in the group of unilateral breast cancer patients (OR, 0.90; 95%CI, 0.83-0.97). 25556434

2014

dbSNP: rs895819
rs895819
0.100 GeneticVariation BEFREE Compared with the ancestral T allele in miR-196a2 rs11614913, the variant C allele was consistently associated with an increased risk of breast cancer (odds ratio = 2.20, 95% confidence interval = 1.19-4.09, P < 0.01) and clinical pathological type (P < 0.01). miR-27a rs895819 A>G and miR-499 rs3746444 A>G were not associated with breast cancer risk. 26125831

2015

dbSNP: rs895819
rs895819
0.100 GeneticVariation BEFREE In conclusion, the rs2292832 polymorphism was significantly associated with increased breast cancer</span> risk, and the rs895819 polymorphism contributes to the susceptibility of colorectal and breast cancer. 26993779

2016

dbSNP: rs895819
rs895819
0.100 GeneticVariation BEFREE Our findings support the following conclusions: a) rs6505162:C > A in pre-miR-423 increases risk of familial BC in families with a strong history of BC; b) the C/A genotype at rs2682818:C > A (pre-miR-618) increases BC risk in non-familial early-onset BC; and c) the G/G genotype at rs895819:A > G (miR-27a) reduces BC risk in families with a moderate history of BC. 27421647

2016

dbSNP: rs895819
rs895819
0.100 GeneticVariation BEFREE To summarize, our results indicated that rs895819 was a protective factor for cancer in Caucasians and could increase colorectal cancer risk but decrease breast cancer risk. 28415619

2017

dbSNP: rs895819
rs895819
0.100 GeneticVariation BEFREE Interestingly, the [G] allele of rs895819 was significantly associated with decreased risk of breast cancer (G <i>vs.</i> A: OR = 0.91, 95% CI = 0.86-0.97). 29088869

2017

dbSNP: rs895819
rs895819
0.100 GeneticVariation BEFREE C allele in the variant rs895819 is associated with decreased risk of breast cancer. 29128203

2017

dbSNP: rs895819
rs895819
0.100 GeneticVariation BEFREE Conclusion Our data indicate that miR-146a (rs2910164) and miR-27a (rs895819) variants contribute to breast cancer. 29521182

2018

dbSNP: rs895819
rs895819
0.100 GeneticVariation BEFREE The present study indicates that only the rs895819 polymorphism was associated with BC risk. 29782194

2018

dbSNP: rs895819
rs895819
0.100 GeneticVariation BEFREE Our results suggested that rs895819 polymorphism was correlated with increased risk of colorectal cancer and breast cancer, but not all types of cancer. 31838252

2020