rs12352658
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs12352658(A;A) |
| Make rs12352658(A;G) |
| Make rs12352658(G;G) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 9 |
| Position | 97789486 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs12352658 |
| dbSNP (classic) | rs12352658 |
| ClinGen | rs12352658 |
| ebi | rs12352658 |
| HLI | rs12352658 |
| Exac | rs12352658 |
| Gnomad | rs12352658 |
| Varsome | rs12352658 |
| LitVar | rs12352658 |
| Map | rs12352658 |
| PheGenI | rs12352658 |
| Biobank | rs12352658 |
| 1000 genomes | rs12352658 |
| hgdp | rs12352658 |
| ensembl | rs12352658 |
| geneview | rs12352658 |
| scholar | rs12352658 |
| rs12352658 | |
| pharmgkb | rs12352658 |
| gwascentral | rs12352658 |
| openSNP | rs12352658 |
| 23andMe | rs12352658 |
| SNPshot | rs12352658 |
| SNPdbe | rs12352658 |
| MSV3d | rs12352658 |
| GWAS Ctlg | rs12352658 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 25918370
] Multiple functional variants in long-range enhancer elements contribute to the risk of SNP rs965513 in thyroid cancer
