rs7911488
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs7911488(A;A) |
| Make rs7911488(A;G) |
| Make rs7911488(G;G) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 10 |
| Position | 103394332 |
| Gene | MIR1307, USMG5 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs7911488 |
| dbSNP (classic) | rs7911488 |
| ClinGen | rs7911488 |
| ebi | rs7911488 |
| HLI | rs7911488 |
| Exac | rs7911488 |
| Gnomad | rs7911488 |
| Varsome | rs7911488 |
| LitVar | rs7911488 |
| Map | rs7911488 |
| PheGenI | rs7911488 |
| Biobank | rs7911488 |
| 1000 genomes | rs7911488 |
| hgdp | rs7911488 |
| ensembl | rs7911488 |
| geneview | rs7911488 |
| scholar | rs7911488 |
| rs7911488 | |
| pharmgkb | rs7911488 |
| gwascentral | rs7911488 |
| openSNP | rs7911488 |
| 23andMe | rs7911488 |
| SNPshot | rs7911488 |
| SNPdbe | rs7911488 |
| MSV3d | rs7911488 |
| GWAS Ctlg | rs7911488 |
| GMAF | 0.2668 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| snp near microRNA | |
|---|---|
| ACC | MI0006444 |
| ID | hsa-mir-1307 |
| offset | -5 |
[PMID 19458495
] Comprehensive analysis of the impact of SNPs and CNVs on human microRNAs and their regulatory genes.
[PMID 19680542] Tissue effect on genetic control of transcript isoform variation.
[PMID 20011102] Fine-scale variation and genetic determinants of alternative splicing across individuals.
[PMID 25977444] The polymorphic terminal-loop of pre-miR-1307 binding with MBNL1 contributes to colorectal carcinogenesis via interference with Dicer1 recruitment
