rs273585634
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs273585634(G;T) |
| Make rs273585634(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 16 |
| Position | 88429948 |
| Gene | ZNF469 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs273585634 |
| dbSNP (classic) | rs273585634 |
| ClinGen | rs273585634 |
| ebi | rs273585634 |
| HLI | rs273585634 |
| Exac | rs273585634 |
| Gnomad | rs273585634 |
| Varsome | rs273585634 |
| LitVar | rs273585634 |
| Map | rs273585634 |
| PheGenI | rs273585634 |
| Biobank | rs273585634 |
| 1000 genomes | rs273585634 |
| hgdp | rs273585634 |
| ensembl | rs273585634 |
| geneview | rs273585634 |
| scholar | rs273585634 |
| rs273585634 | |
| pharmgkb | rs273585634 |
| gwascentral | rs273585634 |
| openSNP | rs273585634 |
| 23andMe | rs273585634 |
| SNPshot | rs273585634 |
| SNPdbe | rs273585634 |
| MSV3d | rs273585634 |
| GWAS Ctlg | rs273585634 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs273585634(T;T) |
| Alt | rs273585634(T;T) |
| Reference | Rs273585634(G;G) |
| Significance | Probable-Pathogenic |
| Disease | Keratoconus 1 |
| Variation | info |
| Gene | ZNF469 |
| CLNDBN | Keratoconus 1 |
| Reversed | 0 |
| HGVS | NC_000016.9:g.88496356G>T |
| CLNSRC | ClinVar |
| CLNACC | RCV000114776.1, |
