rs2043556
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 |
| Make rs2043556(A;A) |
| Make rs2043556(A;G) |
| Make rs2043556(G;G) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 10 |
| Position | 51299646 |
| Gene | MIR605, PRKG1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2043556 |
| dbSNP (classic) | rs2043556 |
| ClinGen | rs2043556 |
| ebi | rs2043556 |
| HLI | rs2043556 |
| Exac | rs2043556 |
| Gnomad | rs2043556 |
| Varsome | rs2043556 |
| LitVar | rs2043556 |
| Map | rs2043556 |
| PheGenI | rs2043556 |
| Biobank | rs2043556 |
| 1000 genomes | rs2043556 |
| hgdp | rs2043556 |
| ensembl | rs2043556 |
| geneview | rs2043556 |
| scholar | rs2043556 |
| rs2043556 | |
| pharmgkb | rs2043556 |
| gwascentral | rs2043556 |
| openSNP | rs2043556 |
| 23andMe | rs2043556 |
| SNPshot | rs2043556 |
| SNPdbe | rs2043556 |
| MSV3d | rs2043556 |
| GWAS Ctlg | rs2043556 |
| GMAF | 0.2759 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| snp near microRNA | |
|---|---|
| ACC | MI0003618 |
| ID | hsa-mir-605 |
| offset | -32 |
[PMID 19458495
] Comprehensive analysis of the impact of SNPs and CNVs on human microRNAs and their regulatory genes.
[PMID 22074121] Associations of miRNA polymorphisms and female physiological characteristics with breast cancer risk in Chinese population.
[PMID 23613771
] Polymorphisms of microRNA Sequences or Binding Sites and Lung Cancer: A Meta-Analysis and Systematic Review
[PMID 24413317
] MicroRNA sequence polymorphisms and the risk of different types of cancer
[PMID 25683625] A functional variant in miR-605 modifies the age of onset in Li-Fraumeni syndrome
[PMID 29221163
] Association of miR-21, miR-126 and miR-605 gene polymorphisms with ischemic stroke risk.
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome 10
- Has genotype
- Has population
- SNP near microRNA
- On chip 23andMe v1
- On chip 23andMe v2
- On chip 23andMe v3
- On chip 23andMe v4
- On chip Affy GenomeWide 6
- On chip Affy500k
- On chip Ancestry v2
- On chip FTDNA2
- On chip FTDNA
- On chip HumanOmni1Quad
- On chip Illumina Human 1M
- On chip Ancestry v2c
- On chip Ancestry v2d
