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