rs2069550
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in clinvar |
| Make rs2069550(C;C) |
| Make rs2069550(C;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 8 |
| Position | 132888141 |
| Gene | TG |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2069550 |
| dbSNP (classic) | rs2069550 |
| ClinGen | rs2069550 |
| ebi | rs2069550 |
| HLI | rs2069550 |
| Exac | rs2069550 |
| Gnomad | rs2069550 |
| Varsome | rs2069550 |
| LitVar | rs2069550 |
| Map | rs2069550 |
| PheGenI | rs2069550 |
| Biobank | rs2069550 |
| 1000 genomes | rs2069550 |
| hgdp | rs2069550 |
| ensembl | rs2069550 |
| geneview | rs2069550 |
| scholar | rs2069550 |
| rs2069550 | |
| pharmgkb | rs2069550 |
| gwascentral | rs2069550 |
| openSNP | rs2069550 |
| 23andMe | rs2069550 |
| SNPshot | rs2069550 |
| SNPdbe | rs2069550 |
| MSV3d | rs2069550 |
| GWAS Ctlg | rs2069550 |
| GMAF | 0.3623 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 19438904] Clinical associations of the genetic variants of CTLA-4, Tg, TSHR, PTPN22, PTPN12 and FCRL3 in patients with Graves' disease
| ClinVar | |
|---|---|
| Risk | rs2069550(C;C) |
| Alt | rs2069550(C;C) |
| Reference | Rs2069550(T;T) |
| Significance | Probable-non-pathogenic |
| Disease | not specified Thyroid dyshormonogenesis |
| Variation | info |
| Gene | TG |
| CLNDBN | not specified Thyroid dyshormonogenesis |
| Reversed | 0 |
| HGVS | NC_000008.10:g.133900386T>C |
| CLNSRC | |
| CLNACC | RCV000246346.1, RCV000331886.1, |
