rs6473
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs6473(A;A) |
| Make rs6473(A;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 32041127 |
| Gene | CYP21A2, TNXB |
| is a | snp |
| is | mentioned by |
| dbSNP | rs6473 |
| dbSNP (classic) | rs6473 |
| ClinGen | rs6473 |
| ebi | rs6473 |
| HLI | rs6473 |
| Exac | rs6473 |
| Gnomad | rs6473 |
| Varsome | rs6473 |
| LitVar | rs6473 |
| Map | rs6473 |
| PheGenI | rs6473 |
| Biobank | rs6473 |
| 1000 genomes | rs6473 |
| hgdp | rs6473 |
| ensembl | rs6473 |
| geneview | rs6473 |
| scholar | rs6473 |
| rs6473 | |
| pharmgkb | rs6473 |
| gwascentral | rs6473 |
| openSNP | rs6473 |
| 23andMe | rs6473 |
| SNPshot | rs6473 |
| SNPdbe | rs6473 |
| MSV3d | rs6473 |
| GWAS Ctlg | rs6473 |
| Max Magnitude | 0 |
[PMID 25249698] CYP21A2 polymorphisms in patients with autoimmune Addison's disease, and linkage disequilibrium to HLA risk alleles
| ClinVar | |
|---|---|
| Risk | rs6473(A;A) rs6473(C;C) |
| Alt | rs6473(A;A) rs6473(C;C) |
| Reference | Rs6473(G;G) |
| Significance | Other |
| Disease | not specified |
| Variation | info |
| Gene | TNXB CYP21A2 |
| CLNDBN | not specified |
| Reversed | 0 |
| HGVS | NC_000006.11:g.32008904G>A |
| CLNSRC | |
| CLNACC | RCV000243232.2, |
