MIR146A, microRNA 146a, 406938

N. diseases: 505; N. variants: 3
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2910164
rs2910164
Entrez Id: 406938;107075116
Gene Symbol: MIR146A;MIR3142HG
MIR146A;MIR3142HG
CUI: C0238463
Disease:
Papillary thyroid carcinoma
0.040 GeneticVariation BEFREE In an association study of 608 PTC patients and 901 controls, we found marked differences in genotype distribution of rs2910164 (P = 0.000002), the GC heterozygous state being associated with an increased risk of acquiring PTC (odds ratio = 1.62, P = 0.000007), and both homozygous states protective with odds ratio = 0.42 for the CC genotype (P = 0.003) and odds ratio = 0.69 for the GG genotype (P = 0.0006). 18474871 2008
dbSNP: rs2910164
rs2910164
Entrez Id: 406938;107075116
Gene Symbol: MIR146A;MIR3142HG
MIR146A;MIR3142HG
CUI: C0919267
Disease:
ovarian neoplasm
0.020 GeneticVariation BEFREE To examine whether rs2910164 plays any role in breast and/or ovarian cancer, we studied associations between this polymorphism and age of diagnosis in 42 patients with familial breast cancer and 82 patients with familial ovarian cancer. 18660546 2008
dbSNP: rs2910164
rs2910164
Entrez Id: 406938;107075116
Gene Symbol: MIR146A;MIR3142HG
MIR146A;MIR3142HG
CUI: C1140680
Disease:
Malignant neoplasm of ovary
0.020 GeneticVariation BEFREE To examine whether rs2910164 plays any role in breast and/or ovarian cancer, we studied associations between this polymorphism and age of diagnosis in 42 patients with familial breast cancer and 82 patients with familial ovarian cancer. 18660546 2008
dbSNP: rs2910164
rs2910164
Entrez Id: 406938;107075116
Gene Symbol: MIR146A;MIR3142HG
MIR146A;MIR3142HG
CUI: C4721610
Disease:
Carcinoma, Ovarian Epithelial
0.020 GeneticVariation BEFREE To examine whether rs2910164 plays any role in breast and/or ovarian cancer, we studied associations between this polymorphism and age of diagnosis in 42 patients with familial breast cancer and 82 patients with familial ovarian cancer. 18660546 2008
dbSNP: rs2910164
rs2910164
Entrez Id: 406938;107075116
Gene Symbol: MIR146A;MIR3142HG
MIR146A;MIR3142HG
CUI: C0010068
Disease:
Coronary heart disease
0.070 GeneticVariation BEFREE We conducted a three-stage case-control study of CHD in Chinese to test our hypothesis by genotyping miR-196a2 rs11614913 and three other pre-miRNA SNPs (miR-146a rs2910164, miR-149 rs2292832, and miR-499 rs3746444) in 1,324 CHD cases and 1,783 non-CHD controls. 19514064 2009
dbSNP: rs2910164
rs2910164
Entrez Id: 406938;107075116
Gene Symbol: MIR146A;MIR3142HG
MIR146A;MIR3142HG
CUI: C0678222
Disease:
Breast Carcinoma
0.100 GeneticVariation BEFREE We compared the genotype and allele frequencies of rs2910164, rs11614913 and rs3746444 in cases versus controls of the German and Italian series, and of the two series combined; we also investigated the effect of the three SNPs on age at breast cancer diagnosis. 19847796 2010
dbSNP: rs2910164
rs2910164
Entrez Id: 406938;107075116
Gene Symbol: MIR146A;MIR3142HG
MIR146A;MIR3142HG
CUI: C0006142
Disease:
Malignant neoplasm of breast
0.100 GeneticVariation BEFREE Recently, the SNPs rs11614913 in hsa-mir-196a2 and rs3746444 in hsa-mir-499 were reported to be associated with increased breast cancer risk, and the SNP rs2910164 in hsa-mir-146a was shown to have an effect on age of breast cancer diagnosis. 19847796 2010
dbSNP: rs2910164
rs2910164
Entrez Id: 406938;107075116
Gene Symbol: MIR146A;MIR3142HG
MIR146A;MIR3142HG
CUI: C0003165
Disease:
Anthracosis
0.010 GeneticVariation BEFREE In a case-control study of 496 CWP patients and 513 control subjects frequency matched by exposure years and work types, we genotyped four single-nucleotide polymorphisms (SNPs) (rs2910164, rs2292832, rs11614913 and rs3746444) in pre-miRNAs (miR-146a, miR-149, miR-196a2 and miR-499) and assessed the associations with risk of CWP. 19881472 2010
dbSNP: rs2910164
rs2910164
Entrez Id: 406938;107075116
Gene Symbol: MIR146A;MIR3142HG
MIR146A;MIR3142HG
CUI: C0600139
Disease:
Prostate carcinoma
0.050 GeneticVariation BEFREE To explore whether rs2910164 plays any role in prostate cancer (CaP), we analyzed the association between miR-146a polymorphism and risk of CaP and the expression of miR-146a with different genotypes in CaP tissues in southern Chinese Han population. 19902466 2010
dbSNP: rs2910164
rs2910164
Entrez Id: 406938;107075116
Gene Symbol: MIR146A;MIR3142HG
MIR146A;MIR3142HG
CUI: C0376358
Disease:
Malignant neoplasm of prostate
0.050 GeneticVariation BEFREE To explore whether rs2910164 plays any role in prostate cancer (CaP), we analyzed the association between miR-146a polymorphism and risk of CaP and the expression of miR-146a with different genotypes in CaP tissues in southern Chinese Han population. 19902466 2010
dbSNP: rs2910164
rs2910164
Entrez Id: 406938;107075116
Gene Symbol: MIR146A;MIR3142HG
MIR146A;MIR3142HG
CUI: C4290046
Disease:
trachomatis
0.010 GeneticVariation BEFREE We investigated whether the SNPs miR-146a G>C (rs2910164), NLRP3 C>T (rs4925663) and G>A (rs12065526) are associated with the susceptibility to and severity of C. trachomatis infection. 20011700 2009
dbSNP: rs2910164
rs2910164
Entrez Id: 406938;107075116
Gene Symbol: MIR146A;MIR3142HG
MIR146A;MIR3142HG
CUI: C1449563
Disease:
Cardiomyopathy, Familial Idiopathic
0.010 GeneticVariation BEFREE Both the has-mir-196a2 rs11614913 C/T and hsa-mir-499 rs3746444 A/G, but not hsa-mir-146a rs2910164 C/G, are associated with a significantly increased risk of DCM, indicating that common genetic polymorphisms in pre-microRNAs are associated with DCM. 20488170 2010
dbSNP: rs2910164
rs2910164
Entrez Id: 406938;107075116
Gene Symbol: MIR146A;MIR3142HG
MIR146A;MIR3142HG
CUI: C4525300
Disease:
Stage IIA Gallbladder Cancer AJCC v8
0.010 GeneticVariation BEFREE Present case-control study evaluated the potential association of three SNPs (rs2910164, rs11614913 and rs3746444) in pre-miRNAs with gallbladder cancer (GBC) risk in 230 GBC cases and 230 controls in a North Indian population. 20520619 2010
dbSNP: rs2910164
rs2910164
Entrez Id: 406938;107075116
Gene Symbol: MIR146A;MIR3142HG
MIR146A;MIR3142HG
CUI: C0153452
Disease:
Malignant neoplasm of gallbladder
0.010 GeneticVariation BEFREE Present case-control study evaluated the potential association of three SNPs (rs2910164, rs11614913 and rs3746444) in pre-miRNAs with gallbladder cancer (GBC) risk in 230 GBC cases and 230 controls in a North Indian population. 20520619 2010
dbSNP: rs2910164
rs2910164
Entrez Id: 406938;107075116
Gene Symbol: MIR146A;MIR3142HG
MIR146A;MIR3142HG
CUI: C0235782
Disease:
Gallbladder Carcinoma
0.010 GeneticVariation BEFREE Present case-control study evaluated the potential association of three SNPs (rs2910164, rs11614913 and rs3746444) in pre-miRNAs with gallbladder cancer (GBC) risk in 230 GBC cases and 230 controls in a North Indian population. 20520619 2010
dbSNP: rs2910164
rs2910164
Entrez Id: 406938;107075116
Gene Symbol: MIR146A;MIR3142HG
MIR146A;MIR3142HG
CUI: C4525301
Disease:
Stage IIB Gallbladder Cancer AJCC v8
0.010 GeneticVariation BEFREE Present case-control study evaluated the potential association of three SNPs (rs2910164, rs11614913 and rs3746444) in pre-miRNAs with gallbladder cancer (GBC) risk in 230 GBC cases and 230 controls in a North Indian population. 20520619 2010
dbSNP: rs2910164
rs2910164
Entrez Id: 406938;107075116
Gene Symbol: MIR146A;MIR3142HG
MIR146A;MIR3142HG
CUI: C4525302
Disease:
Stage III Gallbladder Cancer AJCC v8
0.010 GeneticVariation BEFREE Present case-control study evaluated the potential association of three SNPs (rs2910164, rs11614913 and rs3746444) in pre-miRNAs with gallbladder cancer (GBC) risk in 230 GBC cases and 230 controls in a North Indian population. 20520619 2010
dbSNP: rs2910164
rs2910164
Entrez Id: 406938;107075116
Gene Symbol: MIR146A;MIR3142HG
MIR146A;MIR3142HG
CUI: C4525297
Disease:
Stage 0 Gallbladder Cancer AJCC v8
0.010 GeneticVariation BEFREE Present case-control study evaluated the potential association of three SNPs (rs2910164, rs11614913 and rs3746444) in pre-miRNAs with gallbladder cancer (GBC) risk in 230 GBC cases and 230 controls in a North Indian population. 20520619 2010
dbSNP: rs2910164
rs2910164
Entrez Id: 406938;107075116
Gene Symbol: MIR146A;MIR3142HG
MIR146A;MIR3142HG
CUI: C4525305
Disease:
Stage IV Gallbladder Cancer AJCC v8
0.010 GeneticVariation BEFREE Present case-control study evaluated the potential association of three SNPs (rs2910164, rs11614913 and rs3746444) in pre-miRNAs with gallbladder cancer (GBC) risk in 230 GBC cases and 230 controls in a North Indian population. 20520619 2010
dbSNP: rs2910164
rs2910164
Entrez Id: 406938;107075116
Gene Symbol: MIR146A;MIR3142HG
MIR146A;MIR3142HG
CUI: C1168401
Disease:
Squamous cell carcinoma of the head and neck
0.050 GeneticVariation BEFREE The authors genotyped 4 common polymorphisms in pre-miRNAs: Homo sapiens miRNA 146a (hsa-mir-146a) (reference SNP 2910164 [rs2910164]; guanine to cytosine [G→C]), hsa-mir-149 (rs2292832; guanine to thymine [G→T]), hsa-mir-196a2 (rs11614913; C→T), and hsa-mir-499 (rs3746444; adenine to guanine [A→G]) in 1109 patients with SCCHN (cases) and in 1130 cancer-free patients (controls) in a non-Hispanic white population that was frequency-matched by age and sex. 20549817 2010
dbSNP: rs2910164
rs2910164
Entrez Id: 406938;107075116
Gene Symbol: MIR146A;MIR3142HG
MIR146A;MIR3142HG
CUI: C0006142
Disease:
Malignant neoplasm of breast
0.100 GeneticVariation BEFREE However, no significant association between has-miR-146a rs2910164 polymorphism and breast cancer risk was observed in all comparison models tested. 20640596 2011
dbSNP: rs2910164
rs2910164
Entrez Id: 406938;107075116
Gene Symbol: MIR146A;MIR3142HG
MIR146A;MIR3142HG
CUI: C0678222
Disease:
Breast Carcinoma
0.100 GeneticVariation BEFREE However, no significant association between has-miR-146a rs2910164 polymorphism and breast cancer risk was observed in all comparison models tested. 20640596 2011
dbSNP: rs2910164
rs2910164
Entrez Id: 406938;107075116
Gene Symbol: MIR146A;MIR3142HG
MIR146A;MIR3142HG
CUI: C0279626
Disease:
Squamous cell carcinoma of esophagus
0.040 GeneticVariation BEFREE Compared with rs2910164 variant genotype CC, genotype GG was associated with increased risk of ESCC (Odds Ratio, 2.39, 95% Confidence Interval, 1.36-4.20). 20680470 2010
dbSNP: rs2910164
rs2910164
Entrez Id: 406938;107075116
Gene Symbol: MIR146A;MIR3142HG
MIR146A;MIR3142HG
CUI: C0024623
Disease:
Malignant neoplasm of stomach
0.100 GeneticVariation BEFREE This study aimed to examine the associations of the miR-146a G/C (rs2910164) and TLR4 +3725 G/C (rs11536889) polymorphisms with the risk of Helicobacter pylori (H. pylori) infection, gastric atrophy, and gastric cancer in a Japanese population. 20721625 2011
dbSNP: rs2910164
rs2910164
Entrez Id: 406938;107075116
Gene Symbol: MIR146A;MIR3142HG
MIR146A;MIR3142HG
CUI: C0699791
Disease:
Stomach Carcinoma
0.100 GeneticVariation BEFREE This study aimed to examine the associations of the miR-146a G/C (rs2910164) and TLR4 +3725 G/C (rs11536889) polymorphisms with the risk of Helicobacter pylori (H. pylori) infection, gastric atrophy, and gastric cancer in a Japanese population. 20721625 2011