rs4938723
| Orientation | plus |
| Stabilized | plus |
| Make rs4938723(C;C) |
| Make rs4938723(C;T) |
| Make rs4938723(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 11 |
| Position | 111511840 |
| Gene | BTG4, MIR34B, MIR34C |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4938723 |
| dbSNP (classic) | rs4938723 |
| ClinGen | rs4938723 |
| ebi | rs4938723 |
| HLI | rs4938723 |
| Exac | rs4938723 |
| Gnomad | rs4938723 |
| Varsome | rs4938723 |
| LitVar | rs4938723 |
| Map | rs4938723 |
| PheGenI | rs4938723 |
| Biobank | rs4938723 |
| 1000 genomes | rs4938723 |
| hgdp | rs4938723 |
| ensembl | rs4938723 |
| geneview | rs4938723 |
| scholar | rs4938723 |
| rs4938723 | |
| pharmgkb | rs4938723 |
| gwascentral | rs4938723 |
| openSNP | rs4938723 |
| 23andMe | rs4938723 |
| SNPshot | rs4938723 |
| SNPdbe | rs4938723 |
| MSV3d | rs4938723 |
| GWAS Ctlg | rs4938723 |
| GMAF | 0.3076 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
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[PMID 20309940] A potentially functional polymorphism in the promoter region of miR-34b/c is associated with an increased risk for primary hepatocellular carcinoma
[PMID 23516510
] Associations of pri-miR-34b/c and pre-miR-196a2 Polymorphisms and Their Multiplicative Interactions with Hepatitis B Virus Mutations with Hepatocellular Carcinoma Risk
[PMID 23526039] Association of germline microRNA SNPs in pre-miRNA flanking region and breast cancer risk and survival: the Carolina Breast Cancer Study
[PMID 23632240] Promoter polymorphisms of pri-miR-34b/c are associated with hepatocellular carcinoma
[PMID 24065649] Single-nucleotide polymorphism of the pri-miR-34b/c gene is not associated with susceptibility to congenital heart disease in the Han Chinese population
[PMID 24063968] A causal role for circulating miR-34b in osteosarcoma
[PMID 24194751] Associations of miR-499 and miR-34b/c Polymorphisms with Susceptibility to Hepatocellular Carcinoma: An Evidence-Based Evaluation
[PMID 24337371] Polymorphisms of the pri-miR-34b/c promoter and TP53 codon 72 are associated with risk of colorectal cancer
[PMID 23504554] Interactions of miR-34b/c and TP-53 polymorphisms on the risk of nasopharyngeal carcinoma.
[PMID 25035659] Association between hsa-miR-34b/c rs4938723 T > C promoter polymorphism and cancer risk: a meta-analysis based on 6,036 cases and 6,204 controls
[PMID 25190020] Promoter polymorphisms of miR-34b/c are associated with risk of gastric cancer in a Chinese population
[PMID 25190019] The genetic association between pri-miR-34b/c polymorphism (rs4938723 T > C) and susceptibility to cancers: evidence from published studies
[PMID 25201061] Pri-miR-34b/c rs4938723 TC heterozygote is associated with increased cancer risks: evidence from published data
[PMID 25227823] Association between a Polymorphism in miR-34b/c and Susceptibility to Cancer - a Meta-analysis
[PMID 24945256] Pri-miR-124 rs531564 and pri-miR-34b/c rs4938723 polymorphisms are associated with decreased risk of esophageal squamous cell carcinoma in Chinese populations
[PMID 26402809] Pri-Mir-34b/C and Tp-53 Polymorphisms are Associated With The Susceptibility of Papillary Thyroid Carcinoma: A Case-Control Study
[PMID 28106538] A polymorphism in mir-34b/c as a potential biomarker for early onset of hereditary retinoblastoma.
[PMID 30861198] Association between rs4938723 polymorphism and the risk of primary open-angle glaucoma (POAG) in a Chinese population.
[PMID 31423132] Analysis of association of potentially functional genetic variants within genes encoding miR-34b/c, miR-378 and miR-143/145 with prostate cancer in Serbian population.
[PMID 33544997] Genetic variants and risk of thyroid cancer among Iranian patients.
