rs1317082
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs1317082(A;A) |
| Make rs1317082(A;G) |
| Make rs1317082(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 3 |
| Position | 169779797 |
| Gene | MYNN |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1317082 |
| dbSNP (classic) | rs1317082 |
| ClinGen | rs1317082 |
| ebi | rs1317082 |
| HLI | rs1317082 |
| Exac | rs1317082 |
| Gnomad | rs1317082 |
| Varsome | rs1317082 |
| LitVar | rs1317082 |
| Map | rs1317082 |
| PheGenI | rs1317082 |
| Biobank | rs1317082 |
| 1000 genomes | rs1317082 |
| hgdp | rs1317082 |
| ensembl | rs1317082 |
| geneview | rs1317082 |
| scholar | rs1317082 |
| rs1317082 | |
| pharmgkb | rs1317082 |
| gwascentral | rs1317082 |
| openSNP | rs1317082 |
| 23andMe | rs1317082 |
| SNPshot | rs1317082 |
| SNPdbe | rs1317082 |
| MSV3d | rs1317082 |
| GWAS Ctlg | rs1317082 |
| GMAF | 0.3035 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 23001564 ]
|
| Trait | Telomere length |
| Title | Genome-wide meta-analysis points to CTC1 and ZNF676 as genes regulating telomere homeostasis in humans. |
| Risk Allele | G |
| P-val | 1E-8 |
| Odds Ratio | .07 [0.046-0.089] unit increase |
[PMID 30518759] Variant of SNP rs1317082 at CCSlnc362 (RP11-362K14.5) creates a binding site for miR-4658 and diminishes the susceptibility to CRC.
