Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs4705342
rs4705342
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke
0.020 GeneticVariation BEFREE However, the three other miRNA (miR-143 rs4705342, miR-122 rs17669, and miR-124 r531564) were not associated with IS risk under allele or genotype, nor in different inheritance models. 30895838

2019

dbSNP: rs4705342
rs4705342
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke
0.020 GeneticVariation BEFREE We found for the first time that the rs4705342 CC was a protective factor for IS, probably by reducing the level of miR-145. 27708363

2016

dbSNP: rs17723799
rs17723799
CUI: C0024305
Disease: Lymphoma, Non-Hodgkin
Lymphoma, Non-Hodgkin
0.010 GeneticVariation BEFREE We identified three SNPs in MIR143 that are to be significantly associated with reduced risk of NHL: rs3733846 (odds ratio (OR) [95% confidence interval (CI)] = 0.54 [0.33 ⁻ 0.86], p = 0.010), rs41291957 (OR [95% CI] = 0.61 [0.39 ⁻ 0.94], p = 0.024), and rs17723799 (OR [95% CI] = 0.43 [0.26 ⁻ 0.71], p = 0.0009). 30818878

2019

dbSNP: rs353292
rs353292
CUI: C1853238
Disease: Conotruncal defect
Conotruncal defect
0.010 GeneticVariation BEFREE We investigated the association of these two single-nucleotide polymorphisms (SNPs) in the promoter of <i>miR-143/145</i> (rs353292 and rs4705343) with the susceptibility to CTDs in a Chinese population. 31691635

2019

dbSNP: rs353292
rs353292
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.010 GeneticVariation BEFREE We found that the rs353292 polymorphism was associated with an increased risk for developing CRC in heterozygous comparison (adjusted OR = 1.70, 95% CI, 1.32-2.20, P < 0.001), dominant genetic model (adjusted OR = 1.62, 95% CI, 1.26-2.09, P < 0.001), and allele comparison (adjusted OR = 1.46, 95% CI, 1.16-1.84, P = 0.001). 27444415

2016

dbSNP: rs353292
rs353292
Malignant neoplasm of colon and/or rectum
0.010 GeneticVariation BEFREE A functional variant rs353292 in the flanking region of miR-143/145 contributes to the risk of colorectal cancer. 27444415

2016

dbSNP: rs353293
rs353293
CUI: C0699885
Disease: Carcinoma of bladder
Carcinoma of bladder
0.010 GeneticVariation BEFREE These findings suggest that the functional rs353293 polymorphism may be a useful biomarker to predict the risk of bladder cancer. 27438131

2016

dbSNP: rs353293
rs353293
CUI: C0005695
Disease: Bladder Neoplasm
Bladder Neoplasm
0.010 GeneticVariation BEFREE These findings suggest that the functional rs353293 polymorphism may be a useful biomarker to predict the risk of bladder cancer. 27438131

2016

dbSNP: rs353293
rs353293
Malignant neoplasm of urinary bladder
0.010 GeneticVariation BEFREE These findings suggest that the functional rs353293 polymorphism may be a useful biomarker to predict the risk of bladder cancer. 27438131

2016

dbSNP: rs353293
rs353293
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.010 GeneticVariation BEFREE The mutant genotypes or alleles of rs41291957, rs353292, rs353293, and rs4705341 were significantly associated with an increased risk of CRC compared with the wild genotypes or alleles, while rs4705343, rs17796757, rs3733845, and rs3733846 were significantly associated with a decreased risk of CRC. 23628392

2013

dbSNP: rs41291957
rs41291957
CUI: C0024305
Disease: Lymphoma, Non-Hodgkin
Lymphoma, Non-Hodgkin
0.010 GeneticVariation BEFREE We identified three SNPs in MIR143 that are to be significantly associated with reduced risk of NHL: rs3733846 (odds ratio (OR) [95% confidence interval (CI)] = 0.54 [0.33 ⁻ 0.86], p = 0.010), rs41291957 (OR [95% CI] = 0.61 [0.39 ⁻ 0.94], p = 0.024), and rs17723799 (OR [95% CI] = 0.43 [0.26 ⁻ 0.71], p = 0.0009). 30818878

2019

dbSNP: rs41291957
rs41291957
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.010 GeneticVariation BEFREE However, the association of six polymorphisms (miR-608 rs4919510, miR-499a rs3746444, miR-146a rs2910164, pre-miR-143 rs41291957, pre-miR-124-1 rs531564 and pre-miR-26a-1 rs7372209) with colorectal cancer (CRC) risk, therapeutic response and survival remains unclear. 27713147

2016

dbSNP: rs41291957
rs41291957
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis
0.010 GeneticVariation BEFREE The rs41291957 variant located in the pri-miR-143 sequence is associated with colorectal carcinogenesis. 24752771

2014

dbSNP: rs41291957
rs41291957
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.010 GeneticVariation BEFREE Logistic regression analyses showed no significant association of genotype or allele frequencies of pri-miR-143 rs41291957 A/G polymorphism with the CHD cases in overall or various subtypes compared with the control group. 24752771

2014

dbSNP: rs41291957
rs41291957
CUI: C0152021
Disease: Congenital heart disease
Congenital heart disease
0.010 GeneticVariation BEFREE Therefore, the authors hypothesized that rs41291957 in pri-miR-143 might be involved in the risk of sporadic congenital heart disease (CHD). 24752771

2014

dbSNP: rs41291957
rs41291957
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.010 GeneticVariation BEFREE When stratification analysis was done by different variables, such as tumor size, tumor site, differentiated status, clinical stage, and metastasis status, we found that patients with the mutant allele of rs41291957 had an increased risk to develop a tumor size larger than 5 cm. 23628392

2013

dbSNP: rs41291957
rs41291957
CUI: C0027627
Disease: Neoplasm Metastasis
Neoplasm Metastasis
0.010 GeneticVariation BEFREE When stratification analysis was done by different variables, such as tumor size, tumor site, differentiated status, clinical stage, and metastasis status, we found that patients with the mutant allele of rs41291957 had an increased risk to develop a tumor size larger than 5 cm. 23628392

2013

dbSNP: rs4705342
rs4705342
CUI: C0007766
Disease: Intracranial Aneurysm
Intracranial Aneurysm
0.010 GeneticVariation BEFREE Haplotype of the two loci of rs4705342 and rs4705343 showed that the CT haplotype carried a lower IA risk and higher miR-143 level. 28272526

2017

dbSNP: rs4705342
rs4705342
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
0.010 GeneticVariation BEFREE In conclusion, our findings demonstrate that there is the significant association between the functional promoter variant rs4705342T>C in miR-143 and PCa risk and newly describe the miR-143-KLK2 interaction which provided another potential mechanism for miR-143 anti-tumor function. 25354797

2016

dbSNP: rs4705342
rs4705342
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
0.010 GeneticVariation BEFREE In conclusion, our findings demonstrate that there is the significant association between the functional promoter variant rs4705342T>C in miR-143 and PCa risk and newly describe the miR-143-KLK2 interaction which provided another potential mechanism for miR-143 anti-tumor function. 25354797

2016

dbSNP: rs4705343
rs4705343
CUI: C1853238
Disease: Conotruncal defect
Conotruncal defect
0.010 GeneticVariation BEFREE <b>Results:</b> An association between SNP rs4705343</span> of <i>miR-143/145</i> and CTDs has been confirmed in the Chinese Han population. 31691635

2019

dbSNP: rs4705343
rs4705343
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
0.010 GeneticVariation BEFREE Since miRNA-based mechanisms are shown to be involved in the pathogenesis of prostate cancer (PCa), the aim of the present study was to evaluate the effect of rs4938723, rs1076064 and rs4705343 occurring in regulatory regions of miR-34b/c, miR-143/145 and miR-378, respectively, on PCa risk and progression in Serbian population. 31423132

2019

dbSNP: rs4705343
rs4705343
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
0.010 GeneticVariation BEFREE Since miRNA-based mechanisms are shown to be involved in the pathogenesis of prostate cancer (PCa), the aim of the present study was to evaluate the effect of rs4938723, rs1076064 and rs4705343 occurring in regulatory regions of miR-34b/c, miR-143/145 and miR-378, respectively, on PCa risk and progression in Serbian population. 31423132

2019

dbSNP: rs4705343
rs4705343
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
Non-Small Cell Lung Carcinoma
0.010 GeneticVariation BEFREE Our results indicated that the A allele of rs11134527 might be a risk factor (OR=1.24; 95% CI: 1.03-1.50) and that the T allele of rs4705343 might be a protective factor (OR=0.80; 95% CI: 0.66-0.98) for NSCLC in a Han Chinese population. 29692628

2018

dbSNP: rs4705343
rs4705343
CUI: C0007766
Disease: Intracranial Aneurysm
Intracranial Aneurysm
0.010 GeneticVariation BEFREE Haplotype of the two loci of rs4705342 and rs4705343 showed that the CT haplotype carried a lower IA risk and higher miR-143 level. 28272526

2017