rs2569788
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs2569788(C;C) |
| Make rs2569788(C;G) |
| Make rs2569788(G;G) |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | 19 |
| Position | 10403483 |
| Gene | CDC37, MIR1181 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2569788 |
| dbSNP (classic) | rs2569788 |
| ClinGen | rs2569788 |
| ebi | rs2569788 |
| HLI | rs2569788 |
| Exac | rs2569788 |
| Gnomad | rs2569788 |
| Varsome | rs2569788 |
| LitVar | rs2569788 |
| Map | rs2569788 |
| PheGenI | rs2569788 |
| Biobank | rs2569788 |
| 1000 genomes | rs2569788 |
| hgdp | rs2569788 |
| ensembl | rs2569788 |
| geneview | rs2569788 |
| scholar | rs2569788 |
| rs2569788 | |
| pharmgkb | rs2569788 |
| gwascentral | rs2569788 |
| openSNP | rs2569788 |
| 23andMe | rs2569788 |
| SNPshot | rs2569788 |
| SNPdbe | rs2569788 |
| MSV3d | rs2569788 |
| GWAS Ctlg | rs2569788 |
| Max Magnitude | 0 |
| ? | (C;C) (C;G) (G;G) | 28 |
|---|---|---|
|
| ||
| snp near microRNA | |
|---|---|
| ACC | MI0006274 |
| ID | hsa-mir-1181 |
| offset | 15 |
[PMID 19458495
] Comprehensive analysis of the impact of SNPs and CNVs on human microRNAs and their regulatory genes.
