rs28934580
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | |
| (G;G) | 0 | common in clinvar |
| Make rs28934580(A;A) |
| Make rs28934580(A;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 11 |
| Position | 2166693 |
| Gene | TH |
| is a | snp |
| is | mentioned by |
| dbSNP | rs28934580 |
| dbSNP (classic) | rs28934580 |
| ClinGen | rs28934580 |
| ebi | rs28934580 |
| HLI | rs28934580 |
| Exac | rs28934580 |
| Gnomad | rs28934580 |
| Varsome | rs28934580 |
| LitVar | rs28934580 |
| Map | rs28934580 |
| PheGenI | rs28934580 |
| Biobank | rs28934580 |
| 1000 genomes | rs28934580 |
| hgdp | rs28934580 |
| ensembl | rs28934580 |
| geneview | rs28934580 |
| scholar | rs28934580 |
| rs28934580 | |
| pharmgkb | rs28934580 |
| gwascentral | rs28934580 |
| openSNP | rs28934580 |
| 23andMe | rs28934580 |
| SNPshot | rs28934580 |
| SNPdbe | rs28934580 |
| MSV3d | rs28934580 |
| GWAS Ctlg | rs28934580 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs28934580(A;A) |
| Alt | rs28934580(A;A) |
| Reference | Rs28934580(G;G) |
| Significance | Pathogenic |
| Disease | Segawa syndrome |
| Variation | info |
| Gene | TH |
| CLNDBN | Segawa syndrome, autosomal recessive |
| Reversed | 1 |
| HGVS | NC_000011.9:g.2187923C>T |
| CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
| CLNACC | RCV000013121.16, |
