rs13382089
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in complete genomics |
Make rs13382089(G;T) |
Make rs13382089(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 19 |
Position | 53716600 |
Gene | MIR521-2 |
is a | snp |
is | mentioned by |
dbSNP | rs13382089 |
dbSNP (classic) | rs13382089 |
ClinGen | rs13382089 |
ebi | rs13382089 |
HLI | rs13382089 |
Exac | rs13382089 |
Gnomad | rs13382089 |
Varsome | rs13382089 |
LitVar | rs13382089 |
Map | rs13382089 |
PheGenI | rs13382089 |
Biobank | rs13382089 |
1000 genomes | rs13382089 |
hgdp | rs13382089 |
ensembl | rs13382089 |
geneview | rs13382089 |
scholar | rs13382089 |
rs13382089 | |
pharmgkb | rs13382089 |
gwascentral | rs13382089 |
openSNP | rs13382089 |
23andMe | rs13382089 |
SNPshot | rs13382089 |
SNPdbe | rs13382089 |
MSV3d | rs13382089 |
GWAS Ctlg | rs13382089 |
GMAF | 0.006428 |
Max Magnitude | 0 |
? | (G;G) (G;T) (T;T) | 28 |
---|---|---|
|
snp near microRNA | |
---|---|
ACC | MI0003163 |
ID | hsa-mir-521-2 |
offset | 37 |
[PMID 19458495] Comprehensive analysis of the impact of SNPs and CNVs on human microRNAs and their regulatory genes.