rs45602038
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs45602038(C;C) |
| Make rs45602038(C;T) |
| Make rs45602038(T;T) |
| Reference | GRCh38.p2 38.2/144 |
| Chromosome | 19 |
| Position | 17888430 |
| Gene | SLC5A5 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs45602038 |
| dbSNP (classic) | rs45602038 |
| ClinGen | rs45602038 |
| ebi | rs45602038 |
| HLI | rs45602038 |
| Exac | rs45602038 |
| Gnomad | rs45602038 |
| Varsome | rs45602038 |
| LitVar | rs45602038 |
| Map | rs45602038 |
| PheGenI | rs45602038 |
| Biobank | rs45602038 |
| 1000 genomes | rs45602038 |
| hgdp | rs45602038 |
| ensembl | rs45602038 |
| geneview | rs45602038 |
| scholar | rs45602038 |
| rs45602038 | |
| pharmgkb | rs45602038 |
| gwascentral | rs45602038 |
| openSNP | rs45602038 |
| 23andMe | rs45602038 |
| SNPshot | rs45602038 |
| SNPdbe | rs45602038 |
| MSV3d | rs45602038 |
| GWAS Ctlg | rs45602038 |
| Max Magnitude | 0 |
[PMID 26160439] The potential role of the sodium symporter gene polymorphism in the development of differentiated thyroid cancer
| ClinVar | |
|---|---|
| Risk | rs45602038(T;T) |
| Alt | rs45602038(T;T) |
| Reference | rs45602038(C;C) |
| Significance | Unknown |
| Disease | Thyroid Hormonogenesis Defect |
| Variation | info |
| Gene | SLC5A5 |
| CLNDBN | Thyroid Hormonogenesis Defect |
| Reversed | 0 |
| HGVS | NC_000019.9:g.17999239C>T |
| CLNSRC | |
| CLNACC | RCV000390236.1, |
