rs140124953
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs140124953(A;A) |
| Make rs140124953(A;G) |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | 2 |
| Position | 1494027 |
| Gene | TPO |
| is a | snp |
| is | mentioned by |
| dbSNP | rs140124953 |
| dbSNP (classic) | rs140124953 |
| ClinGen | rs140124953 |
| ebi | rs140124953 |
| HLI | rs140124953 |
| Exac | rs140124953 |
| Gnomad | rs140124953 |
| Varsome | rs140124953 |
| LitVar | rs140124953 |
| Map | rs140124953 |
| PheGenI | rs140124953 |
| Biobank | rs140124953 |
| 1000 genomes | rs140124953 |
| hgdp | rs140124953 |
| ensembl | rs140124953 |
| geneview | rs140124953 |
| scholar | rs140124953 |
| rs140124953 | |
| pharmgkb | rs140124953 |
| gwascentral | rs140124953 |
| openSNP | rs140124953 |
| 23andMe | rs140124953 |
| SNPshot | rs140124953 |
| SNPdbe | rs140124953 |
| MSV3d | rs140124953 |
| GWAS Ctlg | rs140124953 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs140124953(A;A) |
| Alt | rs140124953(A;A) |
| Reference | Rs140124953(G;G) |
| Significance | Pathogenic |
| Disease | Deficiency of iodide peroxidase |
| Variation | info |
| Gene | TPO |
| CLNDBN | Deficiency of iodide peroxidase |
| Reversed | 0 |
| HGVS | NC_000002.11:g.1497799G>A |
| CLNSRC | |
| CLNACC | RCV000414861.1, |
